FDA Inspection 1327254 — Novartis Pharmaceutical Manufacturing GmbH

Novartis Pharmaceutical Manufacturing GmbH — FEI 3027031650

The FDA completed an inspection of Novartis Pharmaceutical Manufacturing GmbH on Oct 10, 2025 in Langkampfen. 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
Oct 10, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Langkampfen (Austria)

Additional Details

Mutual Recognition Agreement (MRA)

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