FDA Inspection 746997 — Baxter Deutschland GmbH

Baxter Deutschland GmbH — FEI 3002806414

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

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