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documents: FDA-2016-D-2565-0001

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2016-D-2565-0001 FDA FDA-2016-D-2565 510(k) Third Party Review Program; Draft Guidance for Industry, Food and Drug Administration Staff, and Third Party Review Organizations; Availability Notice Notice of Availability 2016-09-12T04:00:00Z 2016 9 2016-09-12T04:00:00Z 2016-11-15T04:59:59Z 2016-11-15T02:00:50Z 2016-21876 0 0 09000064821f8301

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