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GUIDANCE DOCUMENT

Exemption from Reporting and Record keeping Requirements for Certain Sunlamp Product Manufacturers September 1981

Final
Docket Number:
FDA-2020-D-0957
Issued by:
Guidance Issuing Office
Center for Devices and Radiological Health

Exemption from Reporting and Recordkeeping Requirements for Certain Sunlamp Product Manufacturers


Submit Comments

You can submit online or written comments on any guidance at any time (see 21 CFR 10.115(g)(5))

If unable to submit comments online, please mail written comments to:

Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852

All written comments should be identified with this document's docket number: FDA-2020-D-0957.

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