FDA Inspection 1246466 — Sandoz GmbH

Sandoz GmbH — FEI 3002806523

The FDA completed an inspection of Sandoz GmbH on November 17, 2023 in Kundl. 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
November 17, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kundl (Austria)

Additional Details

Mutual Recognition Agreement (MRA)