FDA Inspection 1253352 — Astellas Ireland Co Ltd

Astellas Ireland Co Ltd — FEI 3002807020

The FDA completed an inspection of Astellas Ireland Co Ltd on September 2, 2022 in Killorglin. 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
September 2, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Killorglin (Ireland)

Additional Details

Mutual Recognition Agreement (MRA)