documents: FDA-2016-D-2565-0004

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2016-D-2565-0004 FDA FDA-2016-D-2565 Reference 3 - FDA Draft Guidance entitled Accreditation and Reaccreditation Process for Firms under the Third Party Review Program Part I_ 2013 re 510(k) Third Party Review Program; Draft Guidance for Industry, Food and Drug Administration Staff, and Third Party Review Organizations; Availability Supporting & Related Material Background Material 2016-09-12T04:00:00Z 2016 9     2016-09-12T13:37:35Z   0 0 09000064821df16e

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