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withdrawn,object_id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-2011-N-0103-0008,FDA,FDA-2011-N-0103,Microbiology Devices; Classification of In Vitro Diagnostic Devices for Bacillus Species Detection,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-11-17T05:00:00Z,2015,11,2015-11-17T05:00:00Z,2016-02-17T04:59:59Z,2015-12-10T22:00:47Z,2015-29275,0,0,0900006481d4d5ce