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483
•Bloomage Biotechnology Corp., Ltd.•April 26, 2019

Bloomage Biotechnology Corp., Ltd. – FDA 483, Apr 26, 2019

Record Details

An FDA inspection of Bloomage Biotechnology Corp., LTD., an API manufacturer in Jinan, China, revealed significant deficiencies in their quality control systems. Observations included failures in quality unit responsibilities regarding chromatographic data review, inadequate analytical method validation, and incomplete laboratory instrument calibration records. Additionally, the firm did not conduct appropriate laboratory tests for raw materials, intermediates, and APIs.

Company
Bloomage Biotechnology Corp., Ltd.
Inspection date
April 26, 2019
Product type
drugs
Office
Office of Biological Products Operations - Division I
Person
  • Launner Rulon-Torres, CSO
View Company Profile

ID · bbe500a9-bddd-436e-b34a-707edb2d3267

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