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withdrawn,object_id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-2022-N-0150-0008,FDA,FDA-2022-N-0150,"Revocation of Two Authorizations of Emergency Use of In Vitro Diagnostic
Devices for Detection and/or Diagnosis of COVID–19; Availability",Notice,General Notice,2023-03-09T05:00:00Z,2023,3,2023-03-09T05:00:00Z,,2023-03-09T15:45:11Z,2023-04845,0,0,0900006485781d64