FDA Inspection 970201 — Takeda GmbH

Takeda GmbH — FEI 3002806542

The FDA completed an inspection of Takeda GmbH on Apr 22, 2016 in Singen (Hohentwiel). 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
Apr 22, 2016
Fiscal Year
2016
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.