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withdrawn,object_id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-1993-N-0043-0003,FDA,FDA-1993-N-0043,"Adverse Experience Reporting Requirements for Human Drug, Correction",Notice,Correction,1995-01-24T05:00:00Z,1995,1,,,2024-04-29T14:55:05Z,,0,0,09000064804fc3ce