483
Clinical Resolution Laboratory Inc.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.
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ID · e7e13a97-7fd6-45c9-83b7-5a09b128666c
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