FDA Inspection 1233740 — Guerbet Ireland Unlimited Company

Guerbet Ireland Unlimited Company — FEI 1000588788

The FDA completed an inspection of Guerbet Ireland Unlimited Company on June 16, 2023 in Dublin 15. 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 16, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dublin 15 (Ireland)

Additional Details

Mutual Recognition Agreement (MRA)