483
IOI OLEO GMBHIOI OLEO GMBH – FDA 483, Jan 17, 2020
Record Details
IOI OLEO GMBH, a drug substances manufacturer in Witten, Germany, was inspected and cited for significant deficiencies across multiple areas. Observations included inadequate complaint investigations, failure to calibrate manufacturing equipment, improper identification and control of drug substance containers and raw materials, and an incomplete employee training program. These issues indicate a lack of robust quality control and adherence to good manufacturing practices.
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ID · 9eeb8f5e-4e7c-4824-8e2b-17d992f4c5ff
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