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483
•Anhui Hanbon Daily Chemical Co., Ltd.•February 28, 2025

Anhui Hanbon Daily Chemical Co., Ltd. – FDA 483, Feb 28, 2025

Record Details

An FDA inspection of Anhui Hanbon Daily Chemical Co., Ltd., an OTC manufacturer in Huainan, China, revealed significant deficiencies across its quality system, production, and laboratory controls. The firm failed to establish and follow adequate procedures for annual product reviews, process controls, test method validation, raw material identity testing, and stability studies. Additionally, laboratory equipment was not properly qualified or calibrated, indicating a severe lack of control over drug product quality.

Company
Anhui Hanbon Daily Chemical Co., Ltd.
Inspection date
February 28, 2025
Product type
drugs
Office
Office of Inspections and Investigations
Person
  • Vivin George
View Company Profile

ID · 563c7b1b-18c9-4420-85ea-342a1a0cc4f8

Violation Codes1
21 CFR 211.192

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Other documents for Anhui Hanbon Daily Chemical Co., Ltd.
  • 483 - 2017-02-17February 17, 2017
  • 483 - 2016-07-26July 26, 2016

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