[Federal Register Volume 81, Number 176 (Monday, September 12, 2016)]
[Notices]
[Page 62743]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-21877]
[[Page 62743]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2016-N-0628; FDA-2012-N-0306; FDA-2002-N-0323; FDA-
2012-N-0427; FDA-2012-N-0536; FDA-2012-N-0560; FDA-2015-N-3662; FDA-
2012-N-0976; FDA-2013-N-0297; FDA-2012-N-1203; FDA-2011-D-0893; FDA-
2014-N-0189; FDA-2012-N-1210]
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: FDA PRA Staff, Office of Operations,
Food and Drug Administration, Three White Flint North, 11601 Landsdown
St., North Bethesda, MD 20852, [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 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.
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 Associated with New Animal 0910-0032 8/31/2019
Drug Applications......................
Administrative Detention and Banned 0910-0114 8/31/2019
Medical Devices........................
Registration of Food Facilities......... 0910-0502 8/31/2019
Inspection by Accredited Persons Program 0910-0510 8/31/2019
Under the Medical Device User Fee and
Modernization Act of 2002..............
Medical Device User Fee Cover Sheet--FDA 0910-0511 8/31/2019
Form 3601..............................
Guidance on Informed Consent for in 0910-0582 8/31/2019
Vitro Diagnostic Studies Using Leftover
Human Specimens That Are Not
Individually Identifiable..............
Guidance for Reagents for Detection of 0910-0584 8/31/2019
Specific Novel Influenza A Viruses.....
Guidance: Emergency Use Authorization of 0910-0595 8/31/2019
Medical Products.......................
Prevention of Salmonella Enteritidis in 0910-0660 8/31/2019
Shell Eggs During Production--
Recordkeeping and Registration
Provisions.............................
Information to Accompany Humanitarian 0910-0661 8/31/2019
Device Exemption Applications and
Annual Distribution Number Reporting
Requirements...........................
Guidance for Center for Devices and 0910-0738 8/31/2019
Radiological Health Appeals Processes..
Deeming Tobacco Products To Be Subject 0910-0768 8/31/2019
to the FD&C Act........................
Food Labeling: Revision of the Nutrition 0910-0813 7/31/2019
Facts Label and Supplement Facts Label.
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Dated: September 6, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016-21877 Filed 9-9-16; 8:45 am]
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