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483
•GBS Commonwealth Co., Ltd.•February 20, 2020

GBS Commonwealth Co., Ltd. – FDA 483, Feb 20, 2020

Record Details

An FDA inspection of GBS Commonwealth Co., Ltd., a medical device manufacturer in Geumcheon, Seoul, revealed significant deficiencies across its quality system. The firm failed to adequately manage design controls, validate software, evaluate suppliers, control documents, and maintain personnel training records. These issues indicate a systemic lack of adherence to regulatory requirements for medical device manufacturing.

Company
GBS Commonwealth Co., Ltd.
Inspection date
February 20, 2020
Product type
device
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
Person
  • Jude C. Dike
View Company Profile

ID · 5f287841-f7e7-470a-9064-701c3a62cafd

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