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withdrawn,object_id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
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
FDA-2010-D-0226-0021,FDA,FDA-2010-D-0226,"Agency Information Collection Activities; Proposals, Submissions, and Approvals: Draft Guidance on Voluntary Audit Report Submission",Notice,General Notice,2011-07-07T04:00:00Z,2011,7,2011-07-07T04:00:00Z,2011-08-09T03:59:59Z,2011-07-07T15:17:21Z,2011-17051,0,0,0900006480ebb6db
FDA-2010-D-0226-0014,FDA,FDA-2010-D-0226,"AdvaMed Audit Report Format Template, 4/23/2009 - [Advanced Medical Technology Association (AdvaMed) - Comment] re 2010-D-0226-0010",Supporting & Related Material,C-Comment (Supporting and Related Material),2010-07-30T04:00:00Z,2010,7,,,2012-03-24T19:37:07Z,,0,0,0900006480b2142b
FDA-2010-D-0226-0001,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",Notice,NAD-Notice of Availability of Data,2010-05-20T04:00:00Z,2010,5,2010-05-20T04:00:00Z,2010-08-19T03:59:59Z,2010-05-20T14:21:55Z,2010-12098,0,0,0900006480af1400
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