FDA Inspection 1262746 — Novartis Manufacturing LLC

Novartis Manufacturing LLC — FEI 3019881323

The FDA completed an inspection of Novartis Manufacturing LLC on Mar 4, 2025 in Indianapolis, IN. 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
Mar 4, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Indianapolis, IN (United States)