FDA Inspection 1021086 — Novartis Pharma AG

Novartis Pharma AG — FEI 3002807772

The FDA completed an inspection of Novartis Pharma AG on July 6, 2017 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
July 6, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Basel (Switzerland)