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483
•Nippon Protein Co., Ltd. Ashikaga Plant•June 27, 2025

Nippon Protein Co., Ltd. Ashikaga Plant – FDA 483, Jun 27, 2025

Record Details

Nippon Protein Co., Ltd. Ashikaga Plant, an API manufacturer in Japan, received a Form 483 with three observations during an FDA inspection from June 23-27, 2025. The observations primarily concern failures in quality control systems, including inadequate investigations into discrepancies, lack of cleaning validation, and insufficient equipment qualification processes. These issues indicate a moderate level of concern regarding the firm's adherence to good manufacturing practices.

Company
Nippon Protein Co., Ltd. Ashikaga Plant
Inspection date
June 27, 2025
Product type
drugs
Office
Office of Inspections and Investigations
Person
  • Crystal Monroy
View Company Profile

ID · 634252ef-80f9-46ea-b6ce-40a925e2f8e3

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