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483
•Biogen International GmbH•October 9, 2025

Biogen International GmbH – FDA 483, Oct 9, 2025

Record Details

Biogen International GmbH, a drug substance manufacturer in Luterbach, Solothurn, Switzerland, was cited for significant deficiencies in its manufacturing process control, deviation management, cleaning and sanitization, facility maintenance, and gowning procedures. The inspection revealed a lack of process consistency, inadequate evaluation of deviations, and persistent microbial contamination risks. These issues indicate a serious lack of control over critical aspects of drug substance manufacturing.

Company
Biogen International GmbH
Inspection date
October 9, 2025
Product type
drugs
Office
Office of Inspections and Investigations
People
  • Talia A. Faison
  • Milos Dokmanovic (Biologist)
  • Thuy T. Nguyen ( Investigator, Consumer Safety Officer)
  • Mia J. Chang (Pharmaceutical Scientist)
View Company Profile

ID · c41c2586-1c18-4593-b79b-2736eb3f3003

Other documents for Biogen International GmbH
  • EIR - 2023-06-16June 16, 2023
  • 483

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