documents: FDA-2010-D-0605-0005

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0605-0005 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

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