May 6, 2017
Third Party Audit Guidance FDA
This guidance is intended to assist industry and the Food and Drug Administration (FDA) staff by recommending standards
May 5, 2017
FDA Reportable Food Registry
The Reportable Food Registry (RFR or the Registry) was established by Section 1005 of the Food and Drug Administration Amendments Act of 2007 (Pub. L. 110-85)
May 4, 2017
FDA US Enforcement
All recalls monitored by FDA are included in the Enforcement Report once they are classified. Information about how to navigate the report and for definitions of the report labels are found on the Enforcement Report Navigation and Definitions page.
May 3, 2017
How do I interpret an import alert?
If your product is detained without physical examination, you have the right to provide evidence to FDA in an attempt to overcome the appearance of the violation. If you do not provide evidence to FDA, or if the information you provide is not sufficient to overcome the appearance of the violation, your product is subject to refusal into the United States. Visit the Detention and Hearing page for more information on this process.