FDA Inspection 1124409 — Bayer Bitterfeld GmbH

Bayer Bitterfeld GmbH — FEI 3003882513

The FDA completed an inspection of Bayer Bitterfeld GmbH on July 10, 2019 in Bitterfeld-Wolfen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 10, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bitterfeld-Wolfen (Germany)

Additional Details

Mutual Recognition Agreement (MRA)