FDA Inspection 1026805 — Novartis Pharma S.A.S. - Centre De Biotechnologie
The FDA completed an inspection of Novartis Pharma S.A.S. - Centre De Biotechnologie on Sep 12, 2017 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
- Sep 12, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Huningue (France)