FDA Inspection 1207822 — Ipsen Manufacturing Ireland Ltd.

Ipsen Manufacturing Ireland Ltd. — FEI 3002807392

The FDA completed an inspection of Ipsen Manufacturing Ireland Ltd. on Nov 25, 2022 in Dublin 15. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 25, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dublin 15 (Ireland)

Additional Details

Mutual Recognition Agreement (MRA)