FDA Inspection 1126883 — Novartis Manufacturing NV

Novartis Manufacturing NV — FEI 3002037047

The FDA completed an inspection of Novartis Manufacturing NV on November 9, 2018 in Puurs-Sint-Amands. 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 9, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Puurs-Sint-Amands (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)