FDA Inspection 595522 — Takeda GmbH

Takeda GmbH — FEI 3002806542

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

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