documents: FDA-2016-N-3818-0176

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id agency_id docket_id title document_type subtype posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2016-N-3818-0176 FDA FDA-2016-N-3818 Content and Format of Substantial Equivalence Reports; Food and Drug Administration Actions on Substantial Equivalence Reports Rule Final Rule 2021-10-05T04:00:00Z 2021 10 2021-10-05T04:00:00Z   2021-10-05T20:23:28Z 2021-21009 0 0 0900006484dba96e

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