FDA Inspection 1272339 — Bayer Bitterfeld GmbH

Bayer Bitterfeld GmbH — FEI 3003882513

The FDA completed an inspection of Bayer Bitterfeld GmbH on June 19, 2024 in Bitterfeld-Wolfen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 19, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bitterfeld-Wolfen (Germany)

Additional Details

Mutual Recognition Agreement (MRA)