FDA Inspection 1289844 — Novartis Pharma Schweizerhalle Ag

Novartis Pharma Schweizerhalle Ag — FEI 3002865753

The FDA completed an inspection of Novartis Pharma Schweizerhalle Ag on Mar 27, 2025 in Pratteln. 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
Mar 27, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pratteln (Switzerland)

Additional details

Mutual Recognition Agreement (MRA)

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