FDA Inspection 869665 — Takeda GmbH, Plant Oranienburg

Takeda GmbH, Plant Oranienburg — FEI 3002807809

The FDA completed an inspection of Takeda GmbH, Plant Oranienburg on Nov 15, 2013 in Oranienburg. 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
Nov 15, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Oranienburg (Germany)

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