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Form Approved: OMB No. 09100025 Expiration Date: August 31, 2023FORM FDA 3639 (09/20) Guidance for the Submission of Cabinet Ray System Reports Pursuant to 21 CFR 1020.40Public reporting burden for
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The wwwpdffillercom400348951-ucm081625pdf-form form fda 3639 is a form used by the FDA for reporting purposes.
Manufacturers, importers, and distributors of FDA regulated products are required to file the form.
The form should be completed with accurate information about the FDA regulated product being reported.
The purpose of the form is to provide the FDA with information about regulated products.
Information such as product details, manufacturing details, distribution details, and any adverse events must be reported.
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