FDA Issues Warning Letter to Turbare Manufacturing
December 03, 2025
December 03, 2025
WASHINGTON, Dec. 3 -- The U.S. Department of Health and Human Services Food and Drug Administration issued the following warning letter to Turbare Manufacturing from the Center for Drug Evaluation and Research:
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Recipient: Laura Martin, CEO, Turbare Manufacturing, 925 Jeanette Drive, Conway, AR 72032-6651, United States
Issuing Office: Center for Drug Evaluation and Research (CDER), United States
WARNING LETTER
WL # 713516
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Recipient: Laura Martin, CEO, Turbare Manufacturing, 925 Jeanette Drive, Conway, AR 72032-6651, United States
Issuing Office: Center for Drug Evaluation and Research (CDER), United States
WARNING LETTER
WL # 713516
