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483
•Ningxia Qiyuan Pharmaceutical Co., Ltd.•June 25, 2019

Ningxia Qiyuan Pharmaceutical Co., Ltd. – FDA 483, Jun 25, 2019

Record Details

Ningxia Qiyuan Pharmaceutical Co., Ltd., an API manufacturer in Yinchuan, China, was cited for six observations during a June 2019 FDA inspection. Key issues included repeat observations of non-contemporaneous record-keeping, inadequate quality unit responsibilities, insufficient contamination precautions, and poorly detailed cleaning and laboratory procedures. Additionally, the facility's buildings were not properly maintained, with water leaks observed in warehouses.

Company
Ningxia Qiyuan Pharmaceutical Co., Ltd.
Inspection date
June 25, 2019
Product type
drugs
Office
Office of Biological Products Operations - Division I
Person
  • Marijo B. Kambere
View Company Profile

ID · f94bea60-ccfe-4962-946b-dd09d24728ae

Other documents for Ningxia Qiyuan Pharmaceutical Co., Ltd.
  • 483 - 2023-09-12September 12, 2023

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