# CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co. Ltd - Inspection Records

Source: https://www.keypedia.com/companies/cspc-zhongnuo-pharmaceutical-shijiazhuang-co-ltd/31185e73-51d7-4117-8ef0-21b223b24d67

> Inspection records and compliance data for CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co. Ltd in Shijiazhuang, None. Access full analysis and detailed observations.

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## Details

- Name: CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co. Ltd
- FEI Number: 3003196232
- City: Shijiazhuang
- State: None
- Country Name: China
- Address Line 1: Economic, No 57 Yangzi West Rd; Gaocheng
- Zip Code: None
- Business Operations: API MANUFACTURE

## Related Documents

- [483 - CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co. Ltd - 2025-11-11](https://www.keypedia.com/records/483/cspc-zhongnuo-pharmaceutical-shijiazhuang-co-ltd/cb3c576d-a3b4-4b2b-b946-44625f6abff5) — source: FDA, date: November 11, 2025
- [FDA Inspection 1292466 - CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co. Ltd - 2025-11-11](https://www.keypedia.com/records/fda_inspections/cspc-zhongnuo-pharmaceutical-shijiazhuang-co-ltd/4e481189-7cc5-4516-86ff-034ad6970fe6) — classification: Official Action Indicated (OAI), source: FDA, date: November 11, 2025
- [FDA Inspection 1239624 - CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co. Ltd - 2024-08-26](https://www.keypedia.com/records/fda_inspections/cspc-zhongnuo-pharmaceutical-shijiazhuang-co-ltd/8924deda-4b7a-4e67-b813-7adf5a6eff32) — source: FDA, date: August 26, 2024
- [FDA Inspection 921104 - CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co. Ltd - 2015-03-27](https://www.keypedia.com/records/fda_inspections/cspc-zhongnuo-pharmaceutical-shijiazhuang-co-ltd/e1962a79-75bc-441d-9865-0d7a420f5b07) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 27, 2015
- [FDA Inspection 795286 - CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co. Ltd - 2012-07-26](https://www.keypedia.com/records/fda_inspections/cspc-zhongnuo-pharmaceutical-shijiazhuang-co-ltd/e6ecf586-62d9-4288-bb92-c3718175b247) — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2012

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