FDA Inspection 1173120 — Novartis Pharma S.A.S. - Centre de Biotechnologie

Novartis Pharma S.A.S. - Centre de Biotechnologie — FEI 3004864869

The FDA completed an inspection of Novartis Pharma S.A.S. - Centre de Biotechnologie on November 19, 2020 in Huningue. 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 19, 2020
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Huningue (France)

Additional Details

Mutual Recognition Agreement (MRA)