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withdrawn,object_id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-N-0685-0005,FDA,FDA-2013-N-0685,FDA/ORA - Testimony,Other,Testimony,2013-08-08T04:00:00Z,2013,8,2013-08-08T04:00:00Z,,2013-08-08T21:14:56Z,,0,0,09000064813a691e
FDA-2013-N-0685-0003,FDA,FDA-2013-N-0685,FDA/ORA - Agenda,Other,Agenda,2013-08-08T04:00:00Z,2013,8,2013-08-08T04:00:00Z,,2013-08-08T21:01:09Z,,0,0,09000064813a68a7
FDA-2013-N-0685-0004,FDA,FDA-2013-N-0685,FDA/ORA - Transcript,Other,Transcript(s),2013-08-08T04:00:00Z,2013,8,2013-08-08T04:00:00Z,,2013-08-08T21:03:34Z,,0,0,09000064813a690c
FDA-2013-N-0685-0001,FDA,FDA-2013-N-0685,"Food and Drug Administration Safety and Innovation Act Title VII--Drug Supply Chain; Standards for Admission of Imported Drugs, Registration of Commercial Importers and Good Importer Practices; Notification of Public Meeting; Request for Comments",Proposed Rule,Public Meeting,2013-06-20T04:00:00Z,2013,6,2013-06-20T04:00:00Z,2013-08-13T03:59:59Z,2014-01-14T13:37:38Z,2013-14549,0,0,0900006481333a7e