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withdrawn,object_id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-2012-N-0921-0003,FDA,FDA-2012-N-0921,"Agency Information Collection Activities; Proposed Collection;
Comment Request; Adverse Event Reporting; Electronic Submissions",Notice,60 Day Proposed Information Collection,2015-11-18T05:00:00Z,2015,11,2015-11-18T05:00:00Z,2016-01-20T04:59:59Z,2015-11-18T16:39:20Z,2015-29407,0,0,0900006481d54910