documents: FDA-2010-D-0226-0023

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2010-D-0226-0023 FDA FDA-2010-D-0226 Guidance for Industry, Third Parties and Staff; Medical Device ISO 13485:2003 Voluntary Audit Report Submission Pilot Program Other Guidance 2012-03-19T04:00:00Z 2012 3 2012-03-19T04:00:00Z   2024-11-07T22:35:04Z   1 0 0900006480fdb2bd

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