-
Start Preamble
AGENCY:
Animal and Plant Health Inspection Service, USDA.
ACTION:
Final rule.
SUMMARY:
We are amending the regulations to increase the user fees for the veterinary diagnostic services to reflect changes in our operating costs and expenses. We are also setting rates for multiple fiscal years. These actions are necessary to ensure that we recover the actual costs of providing these services. We are also providing for a reasonable balance, or reserve, in the veterinary diagnostics user fee account. The Food, Agriculture, and Conservation Act of 1990, as amended, authorizes us to set and collect these user fees.
DATES:
Effective Date: January 18, 2008.
Start Further InfoFOR FURTHER INFORMATION CONTACT:
For information concerning Veterinary Services (VS) Management Support, Start Printed Page 71745contact Ms. Inez Hockaday, Director, Management Support Staff, VS, APHIS, 4700 River Road Unit 44, Riverdale, MD 20737-1231; (301) 734-7517.
For information concerning VS Program Operations at the National Veterinary Services Laboratory, contact Dr. Elizabeth Lautner, Director, National Veterinary Services Laboratories, 1800 Dayton Road, P.O. Box 844, Ames, IA 50010; (515) 633-7357.
For information concerning user fee rate development, contact Mrs. Kris Caraher, User Fees Section Head, Financial Management Division, MRPBS, APHIS, 4700 River Road Unit 54, Riverdale, MD 20737-1232; (301) 734-5901.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
Background
User fees to reimburse the Animal and Plant Health Inspection Service (APHIS) for the costs of providing veterinary diagnostic services and import and export related services for live animals and birds and animal products are contained in 9 CFR part 130 (referred to below as the regulations). These user fees are authorized by section 2509(c) of the Food, Agriculture, Conservation, and Trade Act of 1990, as amended (21 U.S.C. 136a), which provides that the Secretary of Agriculture may, among other things, prescribe regulations and collect fees to recover the costs of veterinary diagnostics relating to the control and eradication of communicable diseases of livestock or poultry within the United States.
On July 23, 2007, we published in the Federal Register (72 FR 40082-40090, Docket No. APHIS-2006-0161) a proposal [1] to amend the regulations by increasing the user fees for veterinary diagnostic services to reflect changes in our operating costs and changes in calculating our costs, and to establish rates for multiple fiscal years.
We solicited comments concerning our proposal for 60 days ending September 22, 2007. We received one comment by that date, from a private citizen. The commenter supported the proposed rule. Therefore, for the reasons given in the proposed rule, we are adopting the proposed rule as a final rule.
In this final rule, we have made a minor change to the fiscal year 2011 user fees for complement fixation and enzyme-linked immunosorbent assay in § 130.16(a). In the proposed rule, we mistakenly stated that those two fees would be $17 for that year. The correct fee for both tests is $18.
Executive Order 12866 and Regulatory Flexibility Act
This rule has been reviewed under Executive Order 12866. The rule has been determined to be not significant for the purposes of Executive Order 12866 and, therefore, has not been reviewed by the Office of Management and Budget.
Below is a summary of the economic analysis for the changes in APHIS user fees in this final rule. The economic analysis provides a cost-benefit analysis and an analysis of the potential economic effects on small entities as required by the Regulatory Flexibility Act. A copy of the full economic analysis, which includes comparisons of the change in each user fee, may be viewed on the Regulations.gov Web site (see footnote 1 for instructions for accessing Regulations.gov) and may be obtained from the person listed under FOR FURTHER INFORMATION CONTACT.
APHIS is updating the user fees covering the costs of providing veterinary diagnostics services to take into account the routine increases in the cost of doing business. The costs to operate the Veterinary Services Veterinary Diagnostics Program at National Veterinary Services Laboratory increase slightly from year to year due to increases in employee costs (cost of living increases, etc.) and other operational costs. These fees are necessary to provide for full-cost recovery of Agency activities.
Calculating the potential impacts of these changes to the veterinary diagnostics user fees is hindered by the difficulty in determining the elasticities of demand for the covered services. Therefore, Government savings are assumed equivalent to the total user fee collections for each category associated with the rule.
Veterinary diagnostic services and products are provided to animal importers and exporters, veterinarians, State and Federal agencies and laboratories, commercial laboratories, educational institutions, and foreign governments.
There is reason to believe that the impact on most users of the changes in this rule would be small. About 76 percent of the fees change in total by $10 or less. The majority should also make only small contributions to the total additional collections and therefore have a minor impact on the users of those materials and services. This is either because the change is small or the projected volume associated with the user fee is small, or both. In addition, user fees are not charged when tests are provided in the context of disease control or eradication programs. Also, in addition to the role they play in protecting American agriculture, veterinary diagnostic services and products facilitate international trade and thereby enhance the business interests of many of those requesting these services.
Nearly 80 percent of the total projected change in collections would come from changes in only 13 of the 146 fees. Only these 13 fee changes are projected to generate $10,000 or more in additional annual collections by the end of the period covered in this rule. Several factors suggest, however, that these fees should also not have a significant impact on users. These fees include small fees applied to a large annual volume of users, large fees but very small volume of users, fees that represent a small percentage of the overall costs associated with a user's output, single fees for reagents with numerous final users, and fees that enhance the marketability of the user's final output.
To the extent that the changes in user fees would impact operational costs, any entity that utilizes APHIS veterinary diagnostic services and materials could be impacted by the changes. The degree to which an entity could be affected depends on its market power, that is, the extent to which costs are either absorbed or can be passed on to its buyers. Without information on either profit margins or operational expenses of the affected entities, or the effects of changes in operating costs on the affected industry, the scale of the impacts cannot be precisely predicted. However, some conclusions on the overall impacts to domestic and international commerce can be drawn.
If the user fees cannot be passed on, the profit margins of some entities may decline as user fees for veterinary diagnostic services and materials are increased. However, the impacts are expected to be muted. The majority of the changes to the user fees are either small, associated with few users, or both. Over the period covered by the rule, more than 51 percent of the individual increases are $5 or less, more than 76 percent increase by less than $10, and more than 83 percent are associated with fewer than 500 users. The majority should also make only small contributions to the total additional collections and therefore have a minor impact on the users of those services. This is either because the change is small or the projected volume associated with the user fee is small, or both. Even in those instances in which the change in a user fee generates a Start Printed Page 71746larger total increase in collections, the impact should not be significant. This is because they are small fees applied to a large annual volume of users, large fees but applied to a very small volume of users, fees that represent a small percentage of the overall costs associated with a user's output, single fees for reagents with numerous final users, or fees that enhance the marketability of the user's final outputs. Therefore, the increases are not generally expected to substantially reduce profits or impede trade. Indeed, the full burden of the user fee changes is not likely to be borne entirely by the purchasers of veterinary diagnostic services and materials.
Under these circumstances, the Administrator of the Animal and Plant Health Inspection Service has determined that this action will not have a significant economic impact on a substantial number of small entities.
Executive Order 12372
This program/activity is listed in the Catalog of Federal Domestic Assistance under No. 10.025 and is subject to Executive Order 12372, which requires intergovernmental consultation with State and local officials. (See 7 CFR part 3015, subpart V.)
Executive Order 12988
This final rule has been reviewed under Executive Order 12988, Civil Justice Reform. This rule: (1) Preempts all State and local laws and regulations that are inconsistent with this rule; (2) has no retroactive effect; and (3) does not require administrative proceedings before parties may file suit in court challenging this rule.
Paperwork Reduction Act
This final rule contains no new information collection or recordkeeping requirements under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501 et seq.).
Start List of SubjectsList of Subjects in 9 CFR Part 130
- Animals
- Birds
- Diagnostic reagents
- Exports
- Imports
- Poultry and poultry products
- Quarantine
- Reporting and recordkeeping requirements
- Tests
Accordingly, we are amending 9 CFR part 130 as follows:
End Amendment Part Start PartPART 130—USER FEES
End Part Start Amendment Part1. The authority citation for part 130 continues to read as follows:
End Amendment Part Start Amendment Part2. In § 130.15, paragraphs (a) and (b), the tables are revised to read as follows:
End Amendment PartUser fees for veterinary diagnostic isolation and identification tests performed at NVSL (excluding FADDL) or other authorized site.(a) * * *
Test Unit User fee Jan. 18, 2008-Sept. 30, 2008 Oct. 1, 2008-Sept. 30, 2009 Oct. 1, 2009-Sept. 30, 2010 Oct. 1, 2010-Sept. 30, 2011 Beginning Oct. 1, 2011 Bacterial identification, automated Isolate $53.00 $54.00 $55.00 $57.00 $58.00 Bacterial identification, non-automated Isolate 90.00 92.00 94.00 96.00 98.00 Bacterial isolation Sample 36.00 37.00 38.00 39.00 40.00 Bacterial serotyping, all other Isolate 55.00 56.00 56.00 57.00 58.00 Bacterial serotyping, Pasteurella multocida Isolate 18.00 19.00 19.00 19.00 20.00 Bacterial serotyping, Salmonella Isolate 36.00 37.00 38.00 39.00 40.00 Bacterial toxin typing Isolate 120.00 123.00 126.00 128.00 131.00 Bacteriology requiring special characterization Test 92.00 94.00 96.00 98.00 101.00 DNA fingerprinting Test 59.00 61.00 62.00 63.00 64.00 DNA probe Test 83.00 85.00 86.00 88.00 89.00 Fluorescent antibody Test 19.00 19.00 20.00 20.00 20.00 Mycobacterium identification (biochemical) Isolate 115.00 117.00 120.00 122.00 125.00 Mycobacterium identification (gas chromatography) Procedure 96.00 99.00 101.00 103.00 105.00 Mycobacterium isolation, animal inoculations Submission 844.00 852.00 868.00 884.00 900.00 Mycobacterium isolation, all other Submission 151.00 154.00 158.00 161.00 165.00 Mycobacterium paratuberculosis isolation Submission 72.00 74.00 75.00 77.00 79.00 Phage typing, all other Isolate 42.00 43.00 44.00 45.00 46.00 Phage typing, Salmonella enteritidis Isolate 24.00 24.00 25.00 25.00 26.00 (b) * * *
Test Unit User fee Jan. 18, 2008-Sept. 30, 2008 Oct. 1, 2008-Sept. 30, 2009 Oct. 1, 2009-Sept. 30, 2010 Oct. 1, 2010-Sept. 30, 2011 Beginning Oct. 1, 2011 Fluorescent antibody tissue section Test $29.00 $30.00 $30.00 $31.00 $31.00 Virus isolation Test 48.00 49.00 50.00 51.00 52.00 * * * * *3. In § 130.16, paragraphs (a) and (b), the tables are revised to read as follows:
End Amendment PartUser fees for veterinary diagnostic serology tests performed at NVSL (excluding FADDL) or at authorized sites.(a) * * * Start Printed Page 71747
Test Unit User fee Jan. 18, 2008-Sept. 30, 2008 Oct. 1, 2008-Sept. 30, 2009 Oct. 1, 2009-Sept. 30, 2010 Oct. 1, 2010-Sept. 30, 2011 Beginning Oct. 1, 2011 Brucella ring (BRT) Test $36.00 $37.00 $38.00 $39.00 $40.00 Brucella ring, heat inactivated (HIRT) Test 36.00 37.00 38.00 39.00 40.00 Brucella ring, serial (Serial BRT) Test 54.00 56.00 57.00 58.00 59.00 Buffered acidified plate antigen presumptive Test 7.00 7.25 7.50 7.50 8.00 Card Test 4.00 4.00 4.25 4.25 4.50 Complement fixation Test 16.00 17.00 17.00 18.00 18.00 Enzyme linked immunosorbent assay Test 16.00 17.00 17.00 18.00 18.00 Indirect fluorescent antibody Test 14.00 15.00 15.00 15.00 16.00 Microscopic agglutination—includes up to 5 serovars Sample 24.00 24.00 25.00 25.00 26.00 Microscopic agglutination—each serovar in excess of 5 serovars Sample 4.25 4.50 4.50 4.50 4.75 Particle concentration fluorescent immunoassay (PCFIA) Test 36.00 37.00 38.00 38.00 39.00 Plate Test 7.00 7.25 7.50 7.50 7.75 Rapid automated presumptive Test 7.00 7.00 7.25 7.25 7.25 Rivanol Test 7.00 7.25 7.50 7.50 7.75 Tube agglutination Test 7.00 7.25 7.50 7.50 7.75 (b) * * *
Test Unit User fee Jan. 18, 2008-Sept. 30, 2008 Oct. 1, 2008-Sept. 30, 2009 Oct. 1, 2009-Sept. 30, 2010 Oct. 1, 2010-Sept. 30, 2011 Beginning Oct. 1, 2011 Agar gel immunodiffusion Test $16.00 $17.00 $17.00 $17.00 $18.00 Complement fixation Test 16.00 17.00 17.00 18.00 18.00 Enzyme linked immunosorbent assay Test 16.00 17.00 17.00 18.00 18.00 Hemagglutination inhibition Test 14.00 15.00 15.00 15.00 16.00 Indirect fluorescent antibody Test 14.00 15.00 15.00 15.00 16.00 Latex agglutination Test 16.00 17.00 17.00 17.00 18.00 Peroxidase linked antibody Test 15.00 16.00 16.00 16.00 17.00 Plaque reduction neutralization Test 18.00 18.00 19.00 19.00 19.00 Rabies fluorescent antibody neutralization Test 45.00 46.00 47.00 49.00 50.00 Virus neutralization Test 13.00 13.00 14.00 14.00 14.00 * * * * *4. In § 130.17, paragraph (a), the table is revised to read as follows:
End Amendment PartUser fees for other veterinary diagnostic laboratory tests performed at NVSL (excluding FADDL) or at authorized sites.(a) * * *
Test Unit User fee Jan. 18, 2008-Sept. 30, 2008 Oct. 1, 2008-Sept. 30, 2009 Oct. 1, 2009-Sept. 30, 2010 Oct. 1, 2010-Sept. 30, 2011 Beginning Oct. 1, 2011 Aflatoxin quantitation Test $30.00 $31.00 $32.00 $32.00 $33.00 Aflatoxin screen Test 29.00 29.00 30.00 30.00 31.00 Agar gel immunodiffusion spp. identification Test 13.00 13.00 13.00 14.00 14.00 Antibiotic (bioautography) quantitation Test 66.00 67.00 68.00 70.00 72.00 Antibiotic (bioautography) screen Test 119.00 122.00 125.00 128.00 130.00 Antibiotic inhibition Test 66.00 67.00 68.00 70.00 72.00 Arsenic Test 17.00 18.00 18.00 19.00 19.00 Ergot alkaloid screen Test 66.00 67.00 68.00 70.00 72.00 Ergot alkaloid confirmation Test 86.00 88.00 89.00 91.00 94.00 Feed microscopy Test 66.00 67.00 68.00 70.00 72.00 Fumonisin only Test 37.00 38.00 39.00 40.00 40.00 Gossypol Test 98.00 100.00 103.00 105.00 107.00 Mercury Test 145.00 148.00 151.00 155.00 158.00 Metals screen Test 44.00 45.00 46.00 47.00 48.00 Metals single element confirmation Test 13.00 13.00 13.00 14.00 14.00 Mycotoxin: aflatoxin-liver Test 119.00 122.00 125.00 128.00 130.00 Mycotoxin screen Test 48.00 49.00 50.00 51.00 52.00 Nitrate/nitrite Test 66.00 67.00 68.00 70.00 72.00 Start Printed Page 71748 Organic compound confirmation Test 88.00 90.00 92.00 94.00 96.00 Organic compound screen Test 151.00 155.00 158.00 161.00 165.00 Parasitology Test 29.00 29.00 30.00 30.00 31.00 Pesticide quantitation Test 132.00 135.00 138.00 141.00 144.00 Pesticide screen Test 60.00 62.00 63.00 64.00 66.00 pH Test 26.00 27.00 28.00 28.00 29.00 Plate cylinder Test 98.00 100.00 103.00 105.00 107.00 Selenium Test 44.00 45.00 46.00 47.00 48.00 Silicate/carbonate disinfectant Test 66.00 67.00 68.00 70.00 72.00 Temperature disks Test 130.00 133.00 136.00 139.00 142.00 Toxicant quantitation, other Test 110.00 112.00 115.00 117.00 120.00 Toxicant screen, other Test 33.00 33.00 34.00 35.00 36.00 Vomitoxin only Test 53.00 54.00 55.00 56.00 58.00 Water activity Test 33.00 33.00 34.00 35.00 36.00 Zearaleone quantitation Test 53.00 54.00 55.00 56.00 58.00 Zearaleone screen Test 29.00 29.00 30.00 30.00 31.00 * * * * *5. In § 130.18, paragraphs (a) and (b), the tables are revised to read as follows:
End Amendment PartUser fees for veterinary diagnostic reagents produced at NVSL or other authorized site (excluding FADDL).(a) * * *
Reagent Unit User fee Jan. 18, 2008-Sept. 30, 2008 Oct. 1, 2008-Sept. 30, 2009 Oct. 1, 2009-Sept. 30, 2010 Oct. 1, 2010-Sept. 30, 2011 Beginning Oct. 1, 2011 Anaplasma card test antigen 2 mL $95.00 $97.00 $99.00 $101.00 $103.00 Anaplasma card test kit without antigen Kit 127.00 130.00 133.00 136.00 139.00 Anaplasma CF antigen 2 mL 46.00 46.00 46.00 47.00 47.00 Anaplasma stabilate 4.5 mL 175.00 178.00 181.00 185.00 188.00 Avian origin bacterial antiserums 1 mL 48.00 49.00 50.00 51.00 52.00 Bacterial agglutinating antigens other than brucella and salmonella pullorum 5 mL 54.00 55.00 57.00 58.00 59.00 Bacterial conjugates 1 mL 96.00 99.00 101.00 103.00 105.00 Bacterial disease CF antigens, all other 1 mL 29.00 30.00 30.00 31.00 32.00 Bacterial ELISA antigens 1 mL 29.00 30.00 31.00 31.00 32.00 Bacterial or protozoal antiserums, all other 1 mL 60.00 61.00 63.00 64.00 66.00 Bacterial reagent culture1 Culture 73.00 74.00 76.00 78.00 79.00 Bacterial reference culture2 Culture 228.00 233.00 239.00 244.00 249.00 Bacteriophage reference culture Culture 172.00 176.00 180.00 183.00 188.00 Bovine serum factor 1 mL 18.00 18.00 19.00 19.00 19.00 Brucella abortus CF antigen 60 mL 151.00 154.00 158.00 161.00 165.00 Brucella agglutination antigens, all other 60 mL 151.00 154.00 158.00 161.00 165.00 Brucella buffered plate antigen 60 mL 172.00 176.00 180.00 183.00 188.00 Brucella canis tube antigen 25 mL 114.00 116.00 119.00 121.00 124.00 Brucella card test antigen (packaged) Package 90.00 92.00 94.00 96.00 98.00 Brucella card test kit without antigen Kit 113.00 114.00 116.00 117.00 119.00 Brucella cells Gram 19.00 19.00 19.00 20.00 20.00 Brucella cells, dried Pellet 6.00 6.00 6.25 6.25 6.25 Brucella ring test antigen 60 mL 241.00 246.00 252.00 257.00 263.00 Brucella rivanol solution 60 mL 29.00 30.00 31.00 31.00 32.00 Dourine CF antigen 1 mL 89.00 91.00 93.00 95.00 97.00 Dourine stabilate 4.5 mL 109.00 111.00 112.00 114.00 116.00 Equine and bovine origin babesia species antiserums 1 mL 127.00 130.00 133.00 136.00 139.00 Equine negative control CF antigen 1 mL 282.00 283.00 286.00 290.00 293.00 Flazo-orange 3 mL 13.00 13.00 13.00 13.00 14.00 Glanders CF antigen 1 mL 77.00 79.00 81.00 82.00 84.00 Hemoparasitic disease CF antigens, all other 1 mL 541.00 553.00 565.00 577.00 590.00 Leptospira transport medium 10 mL 4.25 4.50 4.50 4.50 4.75 Monoclonal antibody 1 mL 95.00 97.00 99.00 101.00 103.00 Mycobacterium spp. old tuberculin 1 mL 24.00 24.00 25.00 25.00 26.00 Mycobacterium spp. PPD 1 mL 18.00 19.00 19.00 19.00 20.00 Mycoplasma hemagglutination antigens 5 mL 180.00 184.00 188.00 192.00 197.00 Negative control serums 1 mL 18.00 19.00 19.00 19.00 20.00 Rabbit origin bacterial antiserum 1 mL 52.00 53.00 54.00 55.00 56.00 Salmonella pullorum microagglutination antigen 5 mL 15.00 16.00 16.00 16.00 17.00 Start Printed Page 71749 Stabilates, all other 4.5 mL 684.00 690.00 703.00 716.00 730.00 1 A reagent culture is a bacterial culture that has been subcultured one or more times after being tested for purity and identity. It is intended for use as a reagent with a diagnostic test such as the leptospiral agglutination test. 2 A reference culture is a bacterial culture that has been thoroughly tested for purity and identity. It should be suitable as a master seed for future cultures. (b) * * *
Reagent Unit User fee Jan. 18, 2008-Sept. 30, 2008 Oct. 1, 2008-Sept. 30, 2009 Oct. 1, 2009-Sept. 30, 2010 Oct. 1, 2010-Sept. 30, 2011 Beginning Oct. 1, 2011 Antigen, except avian influenza and chlamydia psittaci antigens, any 2 mL $61.00 $62.00 $64.00 $65.00 $67.00 Avian antiserum except avian influenza antiserum, any 2 mL 48.00 49.00 51.00 52.00 53.00 Avian influenza antigen, any 2 mL 33.00 34.00 35.00 36.00 36.00 Avian influenza antiserum, any 6 mL 103.00 105.00 108.00 110.00 113.00 Bovine or ovine serum, any 2 mL 127.00 130.00 133.00 136.00 139.00 Cell culture Flask 151.00 154.00 158.00 161.00 165.00 Chlamydia psittaci spp. of origin monoclonal antibody panel Panel 95.00 96.00 98.00 99.00 101.00 Conjugate, any 1 mL 73.00 75.00 76.00 78.00 80.00 Diluted positive control serum, any 2 mL 24.00 25.00 25.00 26.00 27.00 Equine antiserum, any 2 mL 45.00 46.00 47.00 48.00 49.00 Monoclonal antibody 1 mL 102.00 104.00 106.00 108.00 110.00 Other spp. antiserum, any 1 mL 52.00 52.00 52.00 53.00 53.00 Porcine antiserum, any 2 mL 105.00 108.00 110.00 113.00 115.00 Porcine tissue sets Tissue set 157.00 157.00 158.00 159.00 161.00 Positive control tissues, all 2 cm2 section 60.00 62.00 63.00 65.00 66.00 Rabbit origin antiserum 1 mL 52.00 53.00 54.00 55.00 56.00 Reference virus, any 0.6 mL 180.00 184.00 188.00 193.00 197.00 Viruses (except reference viruses), chlamydia psittaci agent or chlamydia psittaci antigen, any 0.6 mL 30.00 31.00 32.00 32.00 33.00 * * * * *6. In § 130.19, paragraph (a), the table is revised to read as follows:
End Amendment PartUser fees for other veterinary diagnostic services or materials provided at NVSL (excluding FADDL).(a) * * *
Service Unit User fee Jan. 18, 2008-Sept. 30, 2008 Oct. 1, 2008-Sept. 30, 2009 Oct. 1, 2009-Sept. 30, 2010 Oct. 1, 2010-Sept. 30, 2011 Beginning Oct. 1, 2011 Antimicrobial susceptibility test Isolate $105.00 $107.00 $109.00 $112.00 $114.00 Avian safety test Test 4,082.00 4,090.00 4,099.00 4,109.00 4,180.00 Check tests, culture Kit 1 176.00 179.00 182.00 185.00 189.00 Check tests, serology Kit 1 361.00 369.00 377.00 385.00 394.00 Fetal bovine serum safety test Verification 1,119.00 1,122.00 1,134.00 1,147.00 1,160.00 Hourly user fees: 2 Hour Hour 104.00 104.00 108.00 112.00 112.00 Quarter hour Quarter Hour 26.00 26.00 27.00 28.00 28.00 Minimum 30.00 31.00 32.00 33.00 33.00 Manual, brucellosis culture 1 copy 115.00 117.00 120.00 122.00 125.00 Manual, tuberculosis Culture (English or Spanish) 1 copy 172.00 176.00 180.00 183.00 188.00 Manual, Veterinary mycology 1 copy 172.00 176.00 180.00 183.00 188.00 Manuals or standard operating procedure (SOP), all other 1 copy 34.00 35.00 36.00 37.00 37.00 Manuals or SOP, per page 1 page 2.25 2.50 2.50 2.75 2.75 Training (school or technical assistance) Per person per day 332.00 339.00 346.00 354.00 362.00 1 Any reagents required for the check test will be charged separately. Start Printed Page 71750 2 For veterinary diagnostic services for which there is no flat user fee the Hourly rate user fee will be calculated for the actual time required to provide the service. * * * * *Done in Washington, DC, this 13th day of December 2007.
Kevin Shea,
Acting Administrator, Animal and Plant Health Inspection Service.
Footnotes
1. To view the proposed rule and the comment we received, go to http://www.regulations.gov/fdmspublic/component/main?main=DocketDetail&d=APHIS-2006-0161.
Back to Citation[FR Doc. E7-24602 Filed 12-18-07; 8:45 am]
BILLING CODE 3410-34-P
Document Information
- Comments Received:
- 0 Comments
- Published:
- 12/19/2007
- Department:
- Animal and Plant Health Inspection Service
- Entry Type:
- Rule
- Action:
- Final rule.
- Document Number:
- E7-24602
- Pages:
- 71744-71750 (7 pages)
- Docket Numbers:
- Docket No. APHIS-2006-0161
- RINs:
- 0579-AC52
- Topics:
- Animals, Exports, Imports, Poultry and poultry products, Quarantine, Reporting and recordkeeping requirements, Wildlife
- PDF File:
- e7-24602.pdf
- CFR: (5)
- 9 CFR 130.15
- 9 CFR 130.16
- 9 CFR 130.17
- 9 CFR 130.18
- 9 CFR 130.19