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483
•TERUMO YAMAGUCHI CORPORATION•February 21, 2020

TERUMO YAMAGUCHI CORPORATION – FDA 483, Feb 21, 2020

Record Details

An FDA inspection of Terumo Yamaguchi D&D Corporation in Yamaguchi, Japan, a drug product manufacturer, revealed significant deficiencies across multiple areas. These include inadequate aseptic processing controls, unqualified personnel for critical inspections, insufficient validation of sterile hold times, and a deficient environmental monitoring program. The findings indicate a need for comprehensive improvements in quality systems, equipment maintenance, and personnel training to ensure the sterility and quality of drug products.

Company
TERUMO YAMAGUCHI CORPORATION
Inspection date
February 21, 2020
Product type
drugs
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
People
  • Virginia A. Carroll
  • Wayne E. Seifert (Senior Regulatory Specialist)
View Company Profile

ID · da05dabd-7392-4090-ad82-f590ea4131b8

Other documents for TERUMO YAMAGUCHI CORPORATION
  • 483 - 2023-03-30March 30, 2023

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