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withdrawn,object_id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-2010-D-0605-0004,FDA,FDA-2010-D-0605,"Reference 2 - FDA. Report a Problem. How to Report Problems With Products Regulated by FDA, http://www.fda.gov/AboutFDA/ContactFDA/ReportaProblem/default.htm.",Supporting & Related Material,GDL-Guidance,2010-12-16T05:00:00Z,2010,12,,,2010-12-16T20:15:49Z,,0,0,0900006480bb894b
FDA-2010-D-0605-0002,FDA,FDA-2010-D-0605,"Guidance for Industry; Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements Small Entiy Compliance Guide",Other,Guidance,2010-12-16T05:00:00Z,2010,12,2010-12-16T05:00:00Z,,2024-11-07T22:29:06Z,,1,0,0900006480bb8335
FDA-2010-D-0605-0003,FDA,FDA-2010-D-0605,"Reference 1 - FDA. Guidance for Industry: Product Recalls, Including Removals and Corrections, http://www.fda.gov/Safety/Recalls/IndustryGuidance/ucm129259.htm",Supporting & Related Material,GDL-Guidance,2010-12-16T05:00:00Z,2010,12,,,2010-12-16T20:15:47Z,,0,0,0900006480bb8949
FDA-2010-D-0605-0001,FDA,FDA-2010-D-0605,"Small Entity Compliance Guides; Availability, etc.: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements",Notice,NAD-Notice of Availability of Data,2010-12-16T05:00:00Z,2010,12,2010-12-16T05:00:00Z,,2024-11-12T05:00:25Z,2010-31613,1,0,0900006480bb8272
FDA-2010-D-0605-0005,FDA,FDA-2010-D-0605,"Reference 3 - FDA. Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act, http://www.fda.gov/FoodGuidances",Supporting & Related Material,GDL-Guidance,2010-12-16T05:00:00Z,2010,12,,,2010-12-16T20:15:51Z,,0,0,0900006480bb894d