FDA Inspection 1274501 — Bayer Weimar GmbH und Co. KG

Bayer Weimar GmbH und Co. KG — FEI 3002808091

The FDA completed an inspection of Bayer Weimar GmbH und Co. KG on November 24, 2022 in Weimar. 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
November 24, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Weimar (Germany)

Additional Details

Mutual Recognition Agreement (MRA)