87 FR 67 pgs. 20432-20433 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals

Type: NOTICEVolume: 87Number: 67Pages: 20432 - 20433
Docket number: [Docket Nos. FDA-2013-N-1529, FDA-2014-D-0609, FDA-2012-N-0961, FDA-2021-N-1022, FDA-2018-N-4130, and FDA-2018-N-3037]
FR document: [FR Doc. 2022-07394 Filed 4-6-22; 8:45 am]
Agency: Health and Human Services Department
Sub Agency: Food and Drug Administration
Official PDF Version:  PDF Version
Pages: 20432, 20433

[top] page 20432

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2013-N-1529, FDA-2014-D-0609, FDA-2012-N-0961, FDA-2021-N-1022, FDA-2018-N-4130, and FDA-2018-N-3037]

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. page 20433

Title of collection OMB control No. Date approval expires
Reclassification Petitions for Medical Devices 0910-0138 2/28/2025
Pharmaceutical Distribution Supply Chain 0910-0806 2/28/2025
Environmental Impact Considerations 0910-0322 3/31/2025
Reporting Associated with Food Additive Petitions, Investigational Food Additive Files Exemptions, and Declaration of Color Additives on Animal Food Labels 0910-0546 3/31/2025
Recordkeeping Requirements for Microbiological Testing and Corrective Measures for Bottled Water 0910-0658 3/31/2025
Generic Clearance for Quantitative Testing for the Development of FDA Communications (CFSAN) 0910-0865 3/31/2025

Dated: March 30, 2022.

Lauren K. Roth,

Associate Commissioner for Policy.

[FR Doc. 2022-07394 Filed 4-6-22; 8:45 am]

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