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483
•Taizhou Kangping Medical Science And Technology Co., Ltd.•March 14, 2025

Taizhou Kangping Medical Science And Technology Co., Ltd. – FDA 483, Mar 14, 2025

Record Details

An FDA inspection of Taizhou Kangping Medical Science And Technology Co., Ltd., an OTC contract manufacturer in Taizhou, China, revealed significant data integrity issues and systemic failures in cGMP compliance. The firm exhibited deficiencies in laboratory record-keeping, stability programs, process validation, and computer system controls, including repeat observations. These findings indicate a lack of adequate oversight and control over critical manufacturing and quality processes, raising concerns about the quality and reliability of drug products.

Company
Taizhou Kangping Medical Science And Technology Co., Ltd.
Inspection date
March 14, 2025
Product type
drugs
Office
Office of Inspections and Investigations
Person
  • Hung H. Do
View Company Profile

ID · 7436045d-3bef-4177-90bf-6c39e037c22f

Other documents for Taizhou Kangping Medical Science And Technology Co., Ltd.
  • WARNING_LETTER - 2025-03-14March 14, 2025
  • 483 - 2019-03-07March 7, 2019

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