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483
•Takeda Pharmaceutical Company Limited•July 19, 2021

Takeda Pharmaceutical Company Limited – FDA 483, Jul 19, 2021

Record Details

An FDA inspection of Takeda Pharmaceutical Company Limited in Yamaguchi, Japan, a sterile drug product manufacturer, revealed significant deficiencies. The firm failed to ensure process simulation studies were representative of commercial operations and had inadequate environmental monitoring in aseptic areas. Additionally, the quality control unit's investigation oversight was found lacking, and critical controls for incoming materials were not established, leading to foreign particle contamination in drug products.

Company
Takeda Pharmaceutical Company Limited
Inspection date
July 19, 2021
Product type
drugs
Office
Office of Biological Products Operations - Division I
People
  • Vincent Thomas
  • Jose E. Melendez (Quality System Specialist)
View Company Profile

ID · d7328c43-e92f-449d-bccf-293394b50bdc

Other documents for Takeda Pharmaceutical Company Limited
  • 483 - 2023-11-06November 6, 2023
  • 483 - 2023-11-01November 1, 2023
  • 483 - 2023-05-24May 24, 2023
  • EIR - 2019-11-26November 26, 2019
  • 483 - 2019-11-26November 26, 2019

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