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FDA Inspection 966800 — Takeda Manufacturing Italia SPA

Takeda Manufacturing Italia SPA — FEI 3007244131

The FDA completed an inspection of Takeda Manufacturing Italia SPA on January 29, 2016 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
January 29, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cittaducale (Italy)

Facility

Other inspections at this facility

  • 1255480 (VAI Tue Nov 12 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1114886 (VAI Fri Nov 15 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1047390 (VAI Tue Feb 27 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 619606 (VAI Tue Sep 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources