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withdrawn,object_id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-2013-D-0636-0024,FDA,FDA-2013-D-0636,"Agency Information Collection Activities; Proposals, Submissions, and Approvals: Unique Device Identification System",Notice,,2013-12-19T05:00:00Z,2013,12,,,2013-12-19T18:18:35Z,2013-30147,0,0,09000064814cb540
FDA-2013-D-0636-0002,FDA,FDA-2013-D-0636,Global Unique Device Identification Database; Draft Guidance for Industry,Other,Guidance,2013-09-25T04:00:00Z,2013,9,2013-09-25T04:00:00Z,,2024-12-18T02:00:35Z,,1,0,0900006481439be6
FDA-2013-D-0636-0001,FDA,FDA-2013-D-0636,Global Unique Device Identification Database; Draft Guidance for Industry; Availability,Notice,Notice of Availability,2013-09-24T04:00:00Z,2013,9,2013-09-24T04:00:00Z,2013-11-26T04:59:59Z,2013-11-30T21:24:11Z,2013-23058,0,0,090000648143435c