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483
•Patheon Biologics LLC•January 24, 2023

Patheon Biologics LLC – FDA 483, Jan 24, 2023

Record Details

An FDA inspection of Patheon Biologics LLC, a drug substance manufacturer in Saint Louis, MO, revealed significant deficiencies across multiple areas. Observations included inadequate facility cleaning and maintenance leading to mold contamination, insufficient control of manufacturing processes, and incomplete risk assessments for viral contamination. Additionally, issues were noted with the segregation and management of expired raw materials, inadequate maintenance programs, and improper labeling of GMP materials and equipment.

Company
Patheon Biologics LLC
Inspection date
January 24, 2023
Product type
drugs
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
People
  • Dilip D. Devineni
  • Zhang Zhao
  • Richard Ledwidge
  • Bonnie J. Mills, PhD
  • Dilip Devineni (Biologist)
View Company Profile

ID · 873b0edd-030b-43fa-98b0-e9085b4a11de

Other documents for Patheon Biologics LLC
  • 483 - 2024-11-20November 20, 2024
  • 483 - 2023-12-08December 8, 2023
  • 483 - 2023-11-10November 10, 2023
  • EIR - 2023-11-10November 10, 2023
  • EIR - 2023-03-02March 2, 2023

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