FDA Issues Warning Letter to LiquidCapsule Manufacturing
January 07, 2026
January 07, 2026
WASHINGTON, Jan. 7 -- The U.S. Department of Health and Human Services Food and Drug Administration issued the following warning letter to LiquidCapsule Manufacturing LLC from the Center for Drug Evaluation and Research:
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Recipient: Mr. Frederick H. Miller, President, LiquidCapsule Manufacturing, LLC, 9216 Palm River Road, Suite 203, Tampa, FL 33619-4478, United States
Issuing Office: Center for Drug Evaluation and Research (CDER), United States
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Recipient: Mr. Frederick H. Miller, President, LiquidCapsule Manufacturing, LLC, 9216 Palm River Road, Suite 203, Tampa, FL 33619-4478, United States
Issuing Office: Center for Drug Evaluation and Research (CDER), United States
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