documents: FDA-2016-D-2565-0029

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2565-0029 FDA FDA-2016-D-2565 510(k) Third Party Review Program and Third Party Emergency Use Authorization (EUA) Review; Draft Guidance for Industry, Food and Drug Administration Staff, and Third Party Review Organizations; Availability Notice Notice of Availability 2023-12-21T05:00:00Z 2023 12     2023-12-21T17:23:07Z 2023-28095 0 0 090000648634e286

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