FDA Inspection 1324108 — Danipharm A/S

Danipharm A/S — FEI 3002806781

The FDA completed an inspection of Danipharm A/S on November 8, 2023 in Nibe. 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 8, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nibe (Denmark)

Additional Details

Mutual Recognition Agreement (MRA)