[Federal Register Volume 82, Number 214 (Tuesday, November 7, 2017)]
[Notices]
[Page 51635]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-24189]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2013-N-0618; FDA-2013-N-1155; FDA-2010-N-0118; FDA-
2011-N-0655; FDA-2014-N-0086; FDA-2011-N-0144; FDA-2016-N-2836]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approvals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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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.
FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, Office of Operations,
Food and Drug Administration, Three White Flint North, 10A-12M, 11601
Landsdown St., North Bethesda, MD 20852, 301-796-7726,
[email protected].
SUPPLEMENTARY 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
https://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.
Table 1--List of Information Collections Approved By OMB
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OMB control Date approval
Title of collection No. expires
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Reporting and Recordkeeping for 0910-0025 7/31/2020
Electronic Products--General
Requirements...........................
Food Labeling Regulations............... 0910-0381 7/31/2020
Prior Notice of Imported Food Under the 0910-0520 7/31/2020
Public Health Security and Bioterrorism
Preparedness and Response Act of 2002..
Animal Generic Drug User Fee Act Cover 0910-0632 7/31/2020
Sheet..................................
Potential Tobacco Product Violations 0910-0716 7/31/2020
Reporting Form.........................
Voluntary Qualified Importer Program 0910-0840 7/31/2020
Guidance for Industry..................
Donor Risk Assessment Questionnaire for 0910-0841 7/31/2020
the FDA/National Heart, Lung, and Blood
Institute--Sponsored Transfusion-
Transmissible Infectious Monitoring
System.................................
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Dated: November 2, 2017.
Anna K. Abram,
Deputy Commissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2017-24189 Filed 11-6-17; 8:45 am]
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