FDA Inspection 746997 — Baxter Deutschland GmbH

Baxter Deutschland GmbH — FEI 3002806414

The FDA completed an inspection of Baxter Deutschland GmbH on August 26, 2011 in Bielefeld. 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
August 26, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bielefeld (Germany)