FDA Regulatory Attorney, FDA Nutrient Content Claims

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FDA Dietary Supplements

• The 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.
• However, 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 FDAs
  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.
www.giannamore-law.com
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  Coral Gables, Florida 33134 Telephone-
  [phone]
• Email us _at_ - contact_at_giannamore-law.com
• Website- http//giannamore-law.com

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