FDA Inspection 1030331 — Takeda Manufacturing Singapore Pte. Ltd.

Takeda Manufacturing Singapore Pte. Ltd. — FEI 3009153654

The FDA completed an inspection of Takeda Manufacturing Singapore Pte. Ltd. on September 29, 2017 in Singapore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 29, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Singapore (Singapore)