483
DESIGN CATAPULT MANUFACTURING, INC.DESIGN CATAPULT MANUFACTURING, INC. – FDA 483, Aug 19, 2025
Record Details
DESIGN CATAPULT MANUFACTURING, INC., a contract manufacturer, was cited for inadequate documentation of corrective and preventive action activities. The firm failed to document investigation activities used to determine the cause of nonconformities, specifically lacking records for the 5 Why Method investigations. This indicates a deficiency in their quality system documentation practices.
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ID · 8a0daf41-d81e-4926-b003-7b50b607c2d4
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