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withdrawn,object_id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-0710-0019,FDA,FDA-2013-D-0710,"Guidance for Industry Circumstances that Constitute Delaying, Denying, Limiting, or Refusing a Drug or Device Inspection DRAFT GUIDANCE",Other,Guidance,2022-12-16T05:00:00Z,2022,12,2022-12-16T05:00:00Z,2023-02-15T04:59:59Z,2024-11-07T00:45:21Z,,1,0,090000648553c711
FDA-2013-D-0710-0018,FDA,FDA-2013-D-0710,"Circumstances That Constitute Delaying, Denying, Limiting, or Refusing a Drug or Device Inspection; Draft Guidance for Industry, Revision 1; Availability",Notice,Notice of Availability,2022-12-16T05:00:00Z,2022,12,,,2022-12-16T17:50:05Z,2022-27344,0,0,090000648553cabe