FDA Inspection 548970 — Novartis Pharma AG

Novartis Pharma AG — FEI 3002807772

The FDA completed an inspection of Novartis Pharma AG on November 6, 2008 in Basel. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 6, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Basel (Switzerland)

Additional Details

Sponsor, Contract Research Organization