# China NMPA Drug Inspection - Anhui Zehua Traditional Chinese Medicine Pieces Co., Ltd. - Bai Ziren

Source: https://www.globalkeysolutions.net/records/china_drug_inspection/anhui-zehua-traditional-chinese-medicine-pieces-co-ltd/d0f511da-4bda-45e7-bd99-2b8bf05b0e93/
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> China NMPA drug inspection for Anhui Zehua Traditional Chinese Medicine Pieces Co., Ltd. published December 22, 2020. Drug: Bai Ziren. On December 22, 2020, the Guizhou Provincial Drug Administration released its third drug quality announcement of the yea

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## Details

- Record Type: CHINA_DRUG_INSPECTION
- Title: Guizhou Provincial Drug Administration Drug Quality Bulletin (Drug Sampling Inspection Information Announcement) (Issue 3, 2020) (Total Issue 41)
- Company Name: Anhui Zehua Traditional Chinese Medicine Pieces Co., Ltd.
- Publication Date: 2020-12-22
- Drug Name: Bai Ziren
- Inspection Finding: The non-compliance item is [Inspection Item] Rancidity: Acid Value.
- Action Taken: Drug regulatory authorities at all levels will investigate and prosecute cases in accordance with relevant laws and regulations, strengthen supervision, urge offenders to correct illegal activities, and enhance risk prevention and control.
- Summary: On December 22, 2020, the Guizhou Provincial Drug Administration released its third drug quality announcement of the year (Issue 41), identifying quality failures in 10 batches of drugs from eight different manufacturers. The inspections, conducted under the Drug Administration Law of the People's Republic of China and related sampling measures, targeted producers, distributors, and healthcare facilities to ensure public safety.

The non-compliant companies included Guiyang Daosheng Health Industry, Guizhou Jingfeng Injection, Anhui Zehua, Jilin Aodong Taonan Pharmaceutical, Sichuan Gukang, Hunan Honghua, Zhangshu Rende, and Sichuan Yifang. Key violations involved failures to meet chemical standards for active ingredients (such as glycyrrhizin and osthol), excessive moisture levels, rancidity, and issues with extract purity and physical appearance. Notably, some samples raised concerns regarding product authenticity, with one manufacturer denying production of the tested batch.

The regulatory framework cited for these actions includes the Administrative Measures for Drug Quality Sampling Inspection. Following these findings, the Administration has ordered local regulatory departments to investigate and prosecute the responsible parties. The involved companies must correct their illegal activities and implement enhanced risk prevention measures to prevent future quality deviations.

Company: https://www.globalkeysolutions.net/companies/anhui-zehua-traditional-chinese-medicine-pieces-co-ltd/0ec7dfe3-3ceb-4392-9717-3bc9ed7817c7/