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Home » Rulemaking » Guidance for Industry: Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act; Availability

Guidance for Industry: Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act; Availability

Document ID: FDA-2007-D-0372-0009
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: E9-16702
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Details Information

Document Subtype: NAD-Notice of Availability of Data
Received Date: July 13 2009, at 01:33 PM Eastern Daylight Time
Start-End Page: 34024 - 34025
Page Count: 2
Comment Start Date: July 14 2009, at 12:00 AM Eastern Standard Time

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