FDA Inspection 1319844 — Niacet B.V.

Niacet B.V. — FEI 3005533399

The FDA completed an inspection of Niacet B.V. on January 10, 2024 in Tiel. 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
January 10, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tiel (Netherlands)

Additional Details

Mutual Recognition Agreement (MRA)