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FDA Inspection 869665 — Takeda GmbH, Plant Oranienburg

Takeda GmbH, Plant Oranienburg — FEI 3002807809

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

Facility

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FDA data resources