FDA Inspection 1290816 — Argenta Dundee Limited

Argenta Dundee Limited — FEI 3002792064

The FDA completed an inspection of Argenta Dundee Limited on June 5, 2025 in Dundee. 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
June 5, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dundee (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)