FDA Inspection 839990 — Takeda Ireland Limited

Takeda Ireland Limited — FEI 3006687027

The FDA completed an inspection of Takeda Ireland Limited on Jun 20, 2013 in Dublin. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jun 20, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dublin (Ireland)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.