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withdrawn,object_id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-1992-S-0039-0067,FDA,FDA-1992-S-0039,Memo Re Changes to CBER Blood Tissue Facility Registration,Other,Memorandum,2018-09-06T04:00:00Z,2018,9,2018-09-06T04:00:00Z,,2018-09-06T16:55:16Z,,0,0,09000064836b3160
FDA-1992-S-0039-0066,FDA,FDA-1992-S-0039,Registering with CVM’s Electronic Submission System Guidance for Industry,Other,Guidance,2018-05-22T04:00:00Z,2018,5,2018-05-22T04:00:00Z,,2024-11-07T01:26:25Z,,1,0,09000064832b1328