FDA Dietary Supplements ď śThe
FDA has very specific requirements for the labels of the products it regulates, including the supplement facts panels of dietary supplements. In particular, the FDA requires certain statements to be made on the Principal Display Panel (PDP) of many FDA-regulated products, such as the Net Quantity of Contents, Statement of Identity, etc. ď śHowever, it must be noted that the label requirements differ based on product classification.
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FDA Warning Letters FDA-issued
warning letters are usually the FDA’s first course of action against companies for alleged non-compliance with the FFDCA and/or FDA regulations.
Per
the written terms of warning letters, the FDA gives recipients fifteen (15) business days to respond in writing, detailing the specific steps taken to correct violations the FFDCA and accompanying regulations.
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About Us Focusing on food and drug law, The Law Office of Katherine Giannamore, P.A. handles a wide range of regulatory issues, including premarket notifications, or 510(k) submissions, removals from import alerts, reconditioning requests, responses to warning letters and a number of other services.
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2020 Ponce De Leon Blvd., Suite 1101 Coral Gables, Florida 33134 Telephone:- (305) 582-5895 Email us @ :- contact@giannamore-law.com Website:- http://giannamore-law.com
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