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483
•Shiono Finesse Ltd.•June 8, 2018

Shiono Finesse Ltd. – FDA 483, Jun 8, 2018

Record Details

Shiono Finesse, Ltd. in Sakai, Fukui, an API manufacturer, was cited with eight observations during an FDA inspection. The observations highlight significant deficiencies in data integrity, equipment cleaning, maintenance programs, process validation, raw material sampling, change control, supplier qualification, and reserve sample management. These issues indicate a lack of robust quality control and adherence to good manufacturing practices.

Company
Shiono Finesse Ltd.
Inspection date
June 8, 2018
Product type
drugs
Office
Office of Biological Products Operations - Division I
People
  • Yasamin Ameri (Compliance Officer)
  • Masami Hasegawa (President and COO)
View Company Profile

ID · 692fa5aa-e5dc-4ed3-a475-2966cf6c9e60

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