2021-28299. Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
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Start Printed Page 74094
AGENCY:
Food and Drug Administration, HHS.
ACTION:
Notice.
SUMMARY:
The Food and Drug Administration (FDA) is publishing a list of information collections that have been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
Start Further InfoFOR FURTHER INFORMATION CONTACT:
Ila S. Mizrachi, Office of Operations, Food and Drug Administration, Three White Flint North, 10 a.m.-12M, 11601 Landsdown St., North Bethesda, MD 20852, 301-796-7726, PRAStaff@fda.hhs.gov.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
The following is a list of FDA information collections recently approved by OMB under section 3507 of the Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control number and expiration date of OMB approval for each information collection are shown in table 1. Copies of the supporting statements for the information collections are available on the internet at http://www.reginfo.gov/public/do/PRAMain. An Agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number.
Start SignatureTable 1—List of Information Collections Approved By OMB
Title of collection OMB control number Date approval expires Request for Samples and Protocols 0910-0206 9/30/2024 Medical Device Recall Authority 0910-0432 9/30/2024 Survey on the Occurrence of Foodborne Illness Risk Factors in Selected Institutional Foodservice and Retail Food Stores Facility Types 0910-0799 9/30/2024 Human Drug Compounding, Repackaging and Related Activities Regarding Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act 0910-0858 9/30/2024 Dated: December 22, 2021.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2021-28299 Filed 12-28-21; 8:45 am]
BILLING CODE 4164-01-P782
Document Information
- Published:
- 12/29/2021
- Department:
- Food and Drug Administration
- Entry Type:
- Notice
- Action:
- Notice.
- Document Number:
- 2021-28299
- Pages:
- 74094-74094 (1 pages)
- Docket Numbers:
- Docket Nos. FDA-2002-N-0314, FDA-2018-N-0405, FDA-2018-N-0270, and FDA-2021-N-0359
- PDF File:
- 2021-28299.pdf
- Supporting Documents:
- » Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
- » Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Reclassification Petitions for Medical Devices
- » Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Reclassification Petitions for Medical Devices
- » Agency Information Collection Activities; Proposed Collection; Comment Request; Reclassification Petitions for Medical Devices
- » 04 Reference 3 Final Regulatory Impact Analysis - Medical Device Classification Procedures: Incorporating FDA Safety and Innovation Act Procedures
- » 03 Reference 2 Open Public Hearings Guidance - Guidance for the Public, FDA Advisory Committee Members, and FDA Staff: The Open Public Hearing at FDA Advisory Committee Meetings
- » 02 Reference 1 Medical Device Classification Product Codes Guidance for Industry
- » 01 Index to References - Final Rule, Medical Device Classification Procedures: Incorporating FDA Safety and Innovation Act Procedures
- » Medical Device Classification Procedures: Incorporating Food and Drug Administration Safety and Innovation Act Procedures
- » Medical Device Classification Procedures; Change of Address; Technical Amendment