FDA Inspection 1255480 — Takeda Manufacturing Italia SPA

Takeda Manufacturing Italia SPA — FEI 3007244131

The FDA completed an inspection of Takeda Manufacturing Italia SPA on November 12, 2024 in Cittaducale. 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
November 12, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cittaducale (Italy)