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withdrawn,object_id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-0226-0022,FDA,FDA-2010-D-0226,"Guidance for Industry, Third Parties and Staff; Availability: Medical Device ISO 13485:2003 Voluntary Audit Report Submission Pilot Program",Notice,Notice of Availability,2012-03-19T04:00:00Z,2012,3,2012-03-19T04:00:00Z,,2012-03-19T18:51:48Z,2012-06503,0,0,0900006480fdacf6
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