FDA Inspection 1205998 — Sandoz GmbH

Sandoz GmbH — FEI 3004828473

The FDA completed an inspection of Sandoz GmbH on July 11, 2022 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 11, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Langkampfen (Austria)

Additional Details

Mutual Recognition Agreement (MRA)