FDA Inspection 595522 — Takeda GmbH

Takeda GmbH — FEI 3002806542

The FDA completed an inspection of Takeda GmbH on June 10, 2009 in Singen (Hohentwiel). 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
June 10, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Singen (Hohentwiel) (Germany)