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 Nov 19, 2020 in Huningue. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 19, 2020
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Huningue (France)

Additional Details

Mutual Recognition Agreement (MRA)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.