documents: FDA-2010-D-0226-0002

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2010-D-0226-0002 FDA FDA-2010-D-0226 Draft Guidance for Industry, Third Parties and Food and Drug Administration Staff: Medical Device Voluntary Audit Report Submission Program; Availability Other GDL-Guidance (Supporting and Related Materials) 2010-05-20T04:00:00Z 2010 5 2010-05-20T04:00:00Z 2010-08-19T03:59:59Z 2010-05-20T14:25:42Z   0 0 0900006480af1462

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