FDA Inspection 672696 — Novartis Pharma Schweizerhalle Ag

Novartis Pharma Schweizerhalle Ag — FEI 3002865753

The FDA completed an inspection of Novartis Pharma Schweizerhalle Ag on Jul 9, 2010 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
Jul 9, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pratteln (Switzerland)

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