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483
•North China Pharmaceutical Huasheng Co., LTD•August 10, 2018

North China Pharmaceutical Huasheng Co., LTD – FDA 483, Aug 10, 2018

Record Details

An FDA inspection of North China Pharmaceutical Huasheng Co., Ltd., an Active Pharmaceutical Ingredients manufacturer, revealed significant deficiencies across multiple areas. The firm failed to adequately validate critical manufacturing processes, ensure the suitability of water used in API production, and maintain proper cleaning and storage of equipment and utensils. These issues indicate a lack of robust quality control and could compromise product quality.

Company
North China Pharmaceutical Huasheng Co., LTD
Inspection date
August 10, 2018
Product type
drugs
Office
Office of Biological Products Operations - Division I
Person
  • Niketa Patel (Consumer Safety Officer/ORA/OMPTO/TOS)
View Company Profile

ID · 7d264857-93e9-4bf6-9c9e-bc7f34df904c

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