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Form Approved: OMB No. 09100025 Expiration Date: August 31, 2023FORM FDA 3661 (09/20) A Guide for the Submission of an Abbreviated Report on Ray Tables, Cradles, Film Changers or Cassette Holders
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Form FDA 3661 0920 is a document used for the reporting of specific information related to drug substances and excipients intended for human use.
Manufacturers and importers of drug substances are required to file Form FDA 3661 0920.
Form FDA 3661 0920 should be filled out by providing accurate information regarding the drug substances, including identification, quantity, and intended use as per the guidelines provided by the FDA.
The purpose of Form FDA 3661 0920 is to collect essential data to help the FDA monitor and assess the safety and efficacy of drug substances.
The form requires information about the drug substance's name, manufacturer, quantity, and other pertinent details related to its production and usage.
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