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483
•Clinical Resolution Laboratory Inc.•September 29, 2023

Clinical Resolution Laboratory Inc. – FDA 483, Sep 29, 2023

Record Details

Clinical Resolution Laboratory Inc. in Brea, CA, was inspected and cited for significant deficiencies in its manufacturing processes and quality control systems. The inspection revealed failures in establishing adequate production controls, thoroughly investigating discrepancies, maintaining appropriate equipment design, and ensuring reliable supplier analyses. These issues indicate a lack of robust quality assurance for drug product identity, strength, purity, and quality.

Company
Clinical Resolution Laboratory Inc.
Inspection date
September 29, 2023
Product type
drugs
Office
Division of Pharmaceutical Quality Operations IV
Person
  • Bryan A. Galvez (Pharmaceutical investigator)
View Company Profile

ID · e7e13a97-7fd6-45c9-83b7-5a09b128666c

Other documents for Clinical Resolution Laboratory Inc.
  • 483 - 2025-01-16January 16, 2025
  • 483 - 2021-04-27April 27, 2021
  • WARNING_LETTER - 2021-04-27April 27, 2021

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