FDA Inspection 725203 — Novartis Pharmaceuticals Corporation

Novartis Pharmaceuticals Corporation — FEI 3000215618

The FDA completed an inspection of Novartis Pharmaceuticals Corporation on May 12, 2011 in Vacaville, CA. 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: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 12, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Vacaville, CA (United States)

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