FDA Inspection 1124409 — Bayer Bitterfeld GmbH

Bayer Bitterfeld GmbH — FEI 3003882513

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

Inspection details

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

Additional details

Mutual Recognition Agreement (MRA)

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