FDA Inspection 678670 — Sandoz GmbH

Sandoz GmbH — FEI 3004828473

The FDA completed an inspection of Sandoz GmbH on July 29, 2010 in Langkampfen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 29, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Langkampfen (Austria)