# China NMPA Inspection - Guangxi Laibin Xiangjiang Biotechnology Co., Ltd. - May 13, 2019

Source: https://www.globalkeysolutions.net/records/china_inspection/guangxi-laibin-xiangjiang-biotechnology-co-ltd/0c51b746-c2a9-4eeb-81c3-740197177647/
Source feed: China

> China NMPA unannounced inspection for Guangxi Laibin Xiangjiang Biotechnology Co., Ltd. published May 13, 2019. In May 2019, the Guangxi Zhuang Autonomous Region Drug Administration announced the results of unannounced inspections conducted in late April 2019. T

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## Details

- Record Type: CHINA_INSPECTION
- Title: Announcement of the Results of Supervision and Inspection of Cosmetic Manufacturers in Guangxi Zhuang Autonomous Region (Issue 2, 2019)
- Company Name: Guangxi Laibin Xiangjiang Biotechnology Co., Ltd.
- Publication Date: 2019-05-13
- Product Type: Cosmetics
- Summary: In May 2019, the Guangxi Zhuang Autonomous Region Drug Administration announced the results of unannounced inspections conducted in late April 2019. These inspections, conducted under the 2019 Cosmetics Supervision Work Plan and 'Key Points for Cosmetics Production License Inspection,' aimed to strengthen oversight of licensed cosmetics manufacturers in the region. Four companies were issued rectification orders due to various non-compliance issues.

**Guangxi Laibin Xiangjiang Biotechnology Co., Ltd.** was cited for high humidity and mold in its finished product warehouse, rust, improper storage of discarded materials, non-functional production workshop equipment (A/C, differential pressure), and outdated quality management documents from 2013. **Guangxi Xiangzhou Sisi Qingyuan Biotechnology Co., Ltd.** exhibited a lack of personnel training plans, uncontrolled quality management documents, an unfamiliar quality manager, facility hygiene issues (standing water, rust), expired staff health certificates, and inaccurate laboratory records.

**Guangxi Xiangzhou Yidan Biotechnology Co., Ltd.** had deficiencies including missing storage labels for raw materials, absent working status labels for equipment, a non-functional differential pressure device, and no records of water purification filter replacements. Finally, **Guangxi Yaodan Biotechnology Co., Ltd.** demonstrated issues with raw material labeling (missing manufacturer, dates), incomplete sample retention logs, improper storage of food in the reagent refrigerator (which lacked temperature monitoring), non-functional lights, expired hygiene status cards, and unstandardized raw material storage.

All inspected companies were mandated to rectify their identified deficiencies within a specified period and submit comprehensive rectification reports to the Guangxi Zhuang Autonomous Region Drug Administration.

Company: https://www.globalkeysolutions.net/companies/guangxi-laibin-xiangjiang-biotechnology-co-ltd/51c47b57-1b3e-4f67-95e7-3cde693f9eaf/