Notices. Notice
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/register/2016/09/12/2016-21877A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
BILLING CODE 4120-01-P 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. 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, *PRAStaff@fda.hhs.gov.* 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 Title of collection OMB control No. Date approval expires Reporting Associated with New Animal Drug Applications 0910-0032 8/31/2019 Administrative Detention and Banned Medical Devices 0910-0114 8/31/2019 Registration of Food Facilities 0910-0502 8/31/2019 Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002 0910-0510 8/31/2019 Medical Device User Fee Cover Sheet—FDA Form 3601 0910-0511 8/31/2019 Guidance on Informed Consent for in Vitro Diagnostic Studies Using Leftover Human Specimens That Are Not Individually Identifiable 0910-0582 8/31/2019 Guidance for Reagents for Detection of Specific Novel Influenza A Viruses 0910-0584 8/31/2019 Guidance: Emergency Use Authorization of Medical Products 0910-0595 8/31/2019 Prevention of *Salmonella* Enteritidis in Shell Eggs During Production—Recordkeeping and Registration Provisions 0910-0660 8/31/2019 Information to Accompany Humanitarian Device Exemption Applications and Annual Distribution Number Reporting Requirements 0910-0661 8/31/2019 Guidance for Center for Devices and Radiological Health Appeals Processes 0910-0738 8/31/2019 Deeming Tobacco Products To Be Subject to the FD&C Act 0910-0768 8/31/2019 Food Labeling: Revision of the Nutrition Facts Label and Supplement Facts Label 0910-0813 7/31/2019 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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