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withdrawn,object_id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-2016-N-0969-0004,FDA,FDA-2016-N-0969,Revocation of Authorization of Emergency Use of an In Vitro Diagnostic Device for Detection of Zika Virus,Notice,Announcement,2017-06-30T04:00:00Z,2017,6,2017-06-30T04:00:00Z,,2017-06-30T15:20:29Z,2017-13666,0,0,09000064827c0422