FDA Inspection 823111 — Astellas Ireland Co Ltd

Astellas Ireland Co Ltd — FEI 3002807020

The FDA completed an inspection of Astellas Ireland Co Ltd on March 8, 2013 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
March 8, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Killorglin (Ireland)