FDA 483 - TRIUMPH PHARMACEUTICALS INC - January 19, 2023
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An FDA inspection of TRIUMPH PHARMACEUTICALS INC in Saint Louis, MO, revealed significant deficiencies in their quality system for medical device manufacturing. The firm failed to adequately maintain device master records, establish corrective and preventive action procedures, and implement medical device reporting procedures. Additionally, inadequate complaint handling and undocumented supplier evaluations were noted, indicating a broad lack of essential quality controls.
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