483
Corixa CorporationCorixa Corporation – FDA 483, Mar 12, 2026
Record Details
An FDA inspection of Corixa Corporation in Marietta, PA, a drug manufacturer, revealed a deficiency in the system for monitoring environmental conditions in aseptic processing areas. Specifically, the firm failed to properly qualify plates used for environmental monitoring samples at a required incubation temperature. This indicates a lapse in quality control for critical manufacturing processes.
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ID · 19a1395e-e985-4823-85ee-2f1a9c60144c
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