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483
•Dynalabs LLC•September 26, 2019

FDA 483 - Dynalabs LLC - September 26, 2019

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Record Details

DynaLabs LLC, a control testing laboratory in Saint Louis, MO, was cited for significant deficiencies in its quality control and laboratory operations. The inspection revealed that test methods for drug products lacked proper validation for customer-specific formulations, and the stability program was inadequate. Furthermore, deviations from procedures were not consistently recorded or justified, and the Quality Unit was found to be deficient in its responsibilities.

Company
Dynalabs LLC
Inspection Date
September 26, 2019
Product Type
Drugs
Office
Division of Human and Animal Food Operations - West II
People
  • Michael G. Truchan (Investigator)
  • Nicole A. Lloyd
  • Emilie E. Kahn (Regulatory Counsel, CDER Compliance, Office of Manufacturing Quality)
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ID · c42e6665-fe90-4922-8d79-4bb2c5e417a9

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