483
Ajinomoto Althea, Inc.Ajinomoto Althea, Inc. – FDA 483, Aug 7, 2019
Record Details
Ajinomoto Althea, Inc. in San Diego, CA, a sterile drug manufacturer, was cited for two significant issues. The firm's quality control unit failed to consistently reject drug product lots contaminated with stainless steel corrosion particulates. Additionally, investigations into discrepancies and batch failures did not always extend to other potentially affected batches or drug products.
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ID · f4a2b512-1b50-4605-a609-304be78baf30
Violation Codes2
21 CFR 21021 CFR 211
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