97-21293. Agency Information Collection Activities; Submission for OMB Review; Comment Request  

  • [Federal Register Volume 62, Number 155 (Tuesday, August 12, 1997)]
    [Notices]
    [Pages 43169-43170]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 97-21293]
    
    
    =======================================================================
    -----------------------------------------------------------------------
    
    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    [Docket No. 97N-0040]
    
    
    Agency Information Collection Activities; Submission for OMB 
    Review; Comment Request
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
    -----------------------------------------------------------------------
    
    SUMMARY: The Food and Drug Administration (FDA) is announcing that the 
    proposed collection of information listed below has been submitted to 
    the Office of Management and Budget (OMB) for review and clearance 
    under the Paperwork Reduction Act of 1995 (the PRA).
    
    DATES: Submit written comments on the collection of information by 
    September 11, 1997.
    
    ADDRESSES: Submit written comments on the collection of information to 
    the Office of Information and Regulatory Affairs, OMB, New Executive 
    Office
    
    [[Page 43170]]
    
    Bldg., 725 17th St. NW., rm. 10235, Washington, DC 20503, Attn: Desk 
    Officer for FDA.
    
    FOR FURTHER INFORMATION CONTACT: Margaret R. Wolff, Office of 
    Information Resources Management (HFA-250), Food and Drug 
    Administration, 5600 Fishers Lane, rm. 16B-19, Rockville, MD 20857, 
    301-827-1223.
    
    SUPPLEMENTARY INFORMATION: In compliance with section 3507 of the PRA 
    (44 U.S.C. 3507), FDA has submitted the following proposed collection 
    of information to OMB for review and clearance.
    
    Food Safety Survey
    
        Under section 903(b)(2) of the Federal Food, Drug, and Cosmetic Act 
    (21 U.S.C. 393(b)(2)), FDA is authorized to conduct research relating 
    to foods and to conduct educational and public information programs 
    relating to the safety of the nation's food supply. FDA is planning to 
    conduct a consumer survey about food safety under this authority. The 
    food safety survey will provide information about consumers' food 
    safety awareness, knowledge, concerns, and practices. A nationally 
    representative sample of 2,000 adults in households with telephones and 
    cooking facilities will be selected at random and interviewed by 
    telephone. Participation will be voluntary. Detailed information will 
    be obtained about risk perception, perceived sources of food 
    contamination, knowledge of particular micro-organisms, safe care label 
    use, food handling practices, consumption of raw foods from animals, 
    information sources, and perceived foodborne illness experience. Most 
    of the questions asked are identical to ones asked in a 1992-1993 
    survey so that changes over this time period can be assessed.
        FDA estimates the burden of this collection of information as 
    follows:
    
                                            Estimated Annual Reporting Burden                                       
    ----------------------------------------------------------------------------------------------------------------
                                                          Annual                                                    
                   No. of Respondents                  Frequency per   Total Annual      Hours per      Total Hours 
                                                         Response        Responses       Response                   
    ----------------------------------------------------------------------------------------------------------------
    2,000                                                   1           2,000                .5         1,000       
    ----------------------------------------------------------------------------------------------------------------
    There are no operating and maintenance costs or capital costs associated with this information collection.      
    
        This will be a one-time survey. The burden estimate is based on 
    FDA's experience with the 1992-1993 survey mentioned previously.
    
        Dated: August 6, 1997.
    William K. Hubbard,
    Associate Commissioner for Policy Coordination.
    [FR Doc. 97-21293 Filed 8-11-97; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
08/12/1997
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
97-21293
Dates:
Submit written comments on the collection of information by September 11, 1997.
Pages:
43169-43170 (2 pages)
Docket Numbers:
Docket No. 97N-0040
PDF File:
97-21293.pdf