FDA Inspection 613771 — Takeda Global Research & Development

Takeda Global Research & Development — FEI 3004447666

The FDA completed an inspection of Takeda Global Research & Development on Sep 21, 2009 in Lake Forest, IL. 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
Sep 21, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Lake Forest, IL (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)