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483
•Pharbil Waltrop Gmbh•June 6, 2025

Pharbil Waltrop Gmbh – FDA 483, Jun 6, 2025

Record Details

An FDA inspection of Pharbil Waltrop Gmbh in Waltrop, Germany, revealed significant deficiencies in the firm's manufacturing and quality control systems. Observations included incomplete batch production records, specifically regarding product reconciliation, and a failure of the quality unit to detect discrepancies in test data between laboratory journals and certificates of analysis. These findings indicate a lack of adequate control over critical production and quality processes.

Company
Pharbil Waltrop Gmbh
Inspection date
June 6, 2025
Product type
drugs
Office
Office of Inspections and Investigations
Person
  • Youkeun Kim
View Company Profile

ID · 03ff22ea-a3b6-449c-8282-241b63a1c29d

Other documents for Pharbil Waltrop Gmbh
  • 483 - 2020-02-14February 14, 2020

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