---
title: "CHENGDA PHARMA passes FDA on-site inspection"
type: "News"
locale: "en"
url: "https://longbridge.com/en/news/227710415.md"
description: "According to the Zhitong Finance APP, CHENGDA PHARMA announced that from November 11 to 15, 2024, the company underwent a cGMP (current Good Manufacturing Practice) on-site inspection by the U.S. Food and Drug Administration (FDA). The inspection covered six major systems: quality system, materials, production, packaging and labeling, equipment facilities, and laboratory controls. Recently, the company received the on-site inspection report (EIR) issued by the FDA, which indicates that the company has passed this on-site inspection"
datetime: "2025-02-10T08:10:04.000Z"
locales:
  - [zh-CN](https://longbridge.com/zh-CN/news/227710415.md)
  - [en](https://longbridge.com/en/news/227710415.md)
  - [zh-HK](https://longbridge.com/zh-HK/news/227710415.md)
---

# CHENGDA PHARMA passes FDA on-site inspection

According to the Zhitong Finance APP, CHENGDA PHARMA (301201.SZ) announced that from November 11 to 15, 2024, it underwent a cGMP (current Good Manufacturing Practice) on-site inspection by the U.S. Food and Drug Administration (FDA). The inspection covered six major systems: quality system, materials, production, packaging and labeling, equipment facilities, and laboratory controls. Recently, the company received the on-site inspection report (EIR) issued by the FDA, which indicates that the company has passed this on-site inspection

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