84 FR 202 pgs. 55972-55973 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Type: NOTICEVolume: 84Number: 202Pages: 55972 - 55973
Pages: 55972, 55973Docket number: [Docket Nos. FDA-2013-N-0370, FDA-2013-N-0065, FDA-2012-N-0427, FDA-2012-N-0536, FDA-2012-N-0873, FDA-2015-N-3662, FDA-2012-N-0976, FDA-2013-N-0297, FDA-2011-D-0893, and FDA-2019-N-1265]
FR document: [FR Doc. 2019-22803 Filed 10-17-19; 8:45 am]
Agency: Health and Human Services Department
Sub Agency: Food and Drug Administration
Official PDF Version: PDF Version
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2013-N-0370, FDA-2013-N-0065, FDA-2012-N-0427, FDA-2012-N-0536, FDA-2012-N-0873, FDA-2015-N-3662, FDA-2012-N-0976, FDA-2013-N-0297, FDA-2011-D-0893, and FDA-2019-N-1265]
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:
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, PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
[top] 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.
| Title of collection | OMB control No. | Date approval expires |
|---|---|---|
| Export of Medical Devices; Foreign Letters of Approval | 0910-0264 | 8/31/2022 |
| Registration of Food Facilities | 0910-0502 | 8/31/2022 |
| Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002 | 0910-0510 | 8/31/2022 |
| Medical Device User Fee Cover Sheet-Form FDA 3601 | 0910-0511 | 8/31/2022 |
| Bar Code Label Requirement for Human Drug Products and Biological Products | 0910-0537 | 8/31/2022 |
| Guidance on Reagents for Detection of Specific Novel Influenza A Viruses | 0910-0584 | 8/31/2022 |
| Guidance: Emergency Use Authorization of Medical Products and Related Authorities | 0910-0595 | 8/31/2022 |
| Production, Storage, and Transportation of Shell Eggs (preventing Salmonella Enteritidis (SE)) | 0910-0660 | 8/31/2022 |
| Center for Devices and Radiological Health Appeals Processes | 0910-0738 | 8/31/2022 |
| Food Labeling: Nutrition Facts Label and Supplement Facts Labels | 0910-0813 | 8/31/2022 |
Dated: October 10, 2019.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2019-22803 Filed 10-17-19; 8:45 am]
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