FDA Inspection 548970 — Novartis Pharma AG

Novartis Pharma AG — FEI 3002807772

The FDA completed an inspection of Novartis Pharma AG on Nov 6, 2008 in Basel Town. 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 6, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Basel Town (Switzerland)

Additional details

Sponsor, Contract Research Organization

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