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withdrawn,object_id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-0226-0031,FDA,FDA-2010-D-0226,"Reference 4, Notice - Canadian Medical Device Conformity Assessment System",Supporting & Related Material,Reference (external attachments),2015-12-17T05:00:00Z,2015,12,,,2015-12-17T15:58:39Z,,0,0,0900006481db7469
FDA-2010-D-0226-0027,FDA,FDA-2010-D-0226,Medical Device ISO 13485: 2003 Voluntary Audit Report Pilot Program; Termination of Pilot Program; Announcement of the Medical Device Single Audit Program Operational Phase List of References,Supporting & Related Material,List,2015-12-17T05:00:00Z,2015,12,,,2015-12-17T15:48:23Z,,0,0,0900006481db740f
FDA-2010-D-0226-0026,FDA,FDA-2010-D-0226,"Medical Device ISO 13485:2003 Voluntary Audit Report Pilot Program;
Termination of Pilot Program; Announcement of the Medical Device
Single Audit Program Operational Phase",Notice,Notice of Termination,2015-12-17T05:00:00Z,2015,12,2015-12-17T05:00:00Z,,2015-12-17T15:07:46Z,2015-31692,0,0,0900006481db6ac6
FDA-2010-D-0226-0029,FDA,FDA-2010-D-0226,"Reference 2, Medical Device Single Audit Program (MDSAP) Mid-Pilot Status Report",Supporting & Related Material,Reference (internal unless indicated),2015-12-17T05:00:00Z,2015,12,,,2015-12-17T15:52:30Z,,0,0,0900006481db7465
FDA-2010-D-0226-0030,FDA,FDA-2010-D-0226,"Reference 3, Medical Device Single Audit Program (MDSAP) Pilot",Supporting & Related Material,Reference (internal unless indicated),2015-12-17T05:00:00Z,2015,12,,,2015-12-17T15:55:32Z,,0,0,0900006481db7467
FDA-2010-D-0226-0028,FDA,FDA-2010-D-0226,"Reference 1, Guidance for Industry, Third Parties and Food and Drug Administration Staff Medical Device ISO 13485: 2003 Voluntary Audit Report Submission Pilot Program",Supporting & Related Material,Reference (internal unless indicated),2015-12-17T05:00:00Z,2015,12,,,2015-12-17T15:47:18Z,,0,0,0900006481db753e