FDA Inspection 601488 — Sandoz GmbH

Sandoz GmbH — FEI 3002806523

The FDA completed an inspection of Sandoz GmbH on July 8, 2009 in Kundl. 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 8, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kundl (Austria)