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FDA Inspection 598994 — Sandoz GmbH

Sandoz GmbH — FEI 3004828473

The FDA completed an inspection of Sandoz GmbH on July 9, 2009 in Langkampfen. 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 9, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Langkampfen (Austria)

Facility

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