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FDA Inspection
•Takeda Pharmaceutical Company Limited•June 11, 2009

Takeda Pharmaceutical Company Limited – FDA Inspection, Jun 11, 2009

Record Details

This FDA Inspection record concerns Takeda Pharmaceutical Company Limited, with an inspection on June 11, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Takeda Pharmaceutical Company Limited
Inspection Date
June 11, 2009
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 8dab6079-805e-47c4-bb6b-42e310fda99c

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
599120
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 606.160(a)(1)Concurrent documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Takeda Pharmaceutical Company Limited

5
DateClassificationOfficeProject area
July 30, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 15, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 9, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 14, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 9, 2011NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Takeda Pharmaceutical Company Limited
  • FDA Inspection 1099764 - 2019-07-30
  • FDA Inspection 975877 - 2016-06-15
  • FDA Inspection 934717 - 2015-07-09
  • FDA Inspection 844248 - 2013-08-14
  • FDA Inspection 712228 - 2011-03-09

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