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FDA Inspection 934717 — Takeda Pharmaceutical Company Limited

Takeda Pharmaceutical Company Limited — FEI 3006611178

The FDA completed an inspection of Takeda Pharmaceutical Company Limited on July 9, 2015 in Ammon, ID. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 9, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Ammon, ID (United States)

Facility

Other inspections at this facility

  • 1099764 (NAI Tue Jul 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 975877 (NAI Wed Jun 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 844248 (NAI Wed Aug 14 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 712228 (NAI Wed Mar 09 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 599120 (VAI Thu Jun 11 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources