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FDA Inspection
•Takeda Pharmaceutical Company Limited•November 6, 2023

Takeda Pharmaceutical Company Limited – FDA Inspection, Nov 6, 2023

Record Details

This FDA Inspection record concerns Takeda Pharmaceutical Company Limited, with an inspection on November 6, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Takeda Pharmaceutical Company Limited
Inspection Date
November 6, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • David J. Gomes (Issuing Officer)
  • Michele Perry-Williams (FDA Associated Person)
View Company Profile

ID · 01fa4df9-a921-4e9e-be5f-bd7dcb845d86

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1224917
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Takeda Pharmaceutical Company Limited

9
DateClassificationOfficeProject area
May 24, 2023Not classifiedOffice of Inspections and Investigations
July 19, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 26, 2019OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 7, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 30, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for Takeda Pharmaceutical Company Limited
  • FDA Inspection 1218059 - 2023-05-24
  • FDA Inspection 1148832 - 2021-07-19
  • FDA Inspection 1111495 - 2019-11-26
  • FDA Inspection 1033814 - 2017-11-07
  • FDA Inspection 951603 - 2015-10-30

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