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withdrawn,object_id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-2011-D-0893-0002,FDA,FDA-2011-D-0893,Draft Guidances for Industry and Staff Center for Devices and Radiological Health Appeals Processes,Other,Guidance,2011-12-28T05:00:00Z,2011,12,2011-12-28T05:00:00Z,2012-04-27T03:59:59Z,2011-12-28T16:23:06Z,,0,0,0900006480f8a53c
FDA-2011-D-0893-0001,FDA,FDA-2011-D-0893,Draft Guidances for Industry and Staff; Availability: Center for Devices and Radiological Health Appeals Processes,Notice,Notice of Availability,2011-12-28T05:00:00Z,2011,12,2011-12-28T05:00:00Z,2012-04-27T03:59:59Z,2014-01-13T17:39:02Z,2011-33230,0,0,0900006480f8a2c3