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withdrawn,object_id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-0683-0005,FDA,FDA-2013-N-0683,FDA/ORA - Testimony,Other,Testimony,2013-08-08T04:00:00Z,2013,8,2013-08-08T04:00:00Z,,2013-08-08T20:26:08Z,,0,0,09000064813a5f9a
FDA-2013-N-0683-0003,FDA,FDA-2013-N-0683,FDA/ORA - Agenda,Other,Agenda,2013-08-08T04:00:00Z,2013,8,2013-08-08T04:00:00Z,,2013-08-08T19:39:41Z,,0,0,09000064813a5ea2
FDA-2013-N-0683-0004,FDA,FDA-2013-N-0683,FDA/ORA - Transcript,Other,Transcript(s),2013-08-08T04:00:00Z,2013,8,2013-08-08T04:00:00Z,,2013-08-08T19:39:16Z,,0,0,09000064813a5f0c
FDA-2013-N-0683-0001,FDA,FDA-2013-N-0683,"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,2013-06-19T04:00:00Z,2013,6,2013-06-19T04:00:00Z,2013-08-13T03:59:59Z,2014-01-14T13:35:08Z,2013-14549,0,0,0900006481331053