# FDA 483 - Nantong Chanyoo Pharmatech Co., Ltd. - March 22, 2019

Source: https://www.globalkeysolutions.net/records/483/nantong-chanyoo-pharmatech-co-ltd/15f610dd-b79a-4174-9117-e73dce73aa91

> FDA 483 for Nantong Chanyoo Pharmatech Co., Ltd. on March 22, 2019. Product: drugs. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: Nantong Chanyoo Pharmatech Co., Ltd.
- Inspection Date: 2019-03-22
- Product Type: drugs
- Office Name: International Compliance Team
- Summary: An FDA inspection of Nantong Chanyoo Pharmatech Co., LTD, an API manufacturer in Nantong, Jiangsu Province, revealed significant deficiencies. Observations included inadequate equipment maintenance and calibration, lack of proper preventative maintenance procedures, and poor facility repair. Additionally, the firm's material system and inventory records were found to be inaccurate.

## Related Officers

- [Investigator](https://www.globalkeysolutions.net/people/michele-perry-williams/80741e95-8df3-41c9-b9b8-499fcb97921d)

Company: https://www.globalkeysolutions.net/companies/nantong-chanyoo-pharmatech-co-ltd/ccfeb4b8-1b9a-4c2c-a01f-f1afcf289155

Office: https://www.globalkeysolutions.net/offices/international-compliance-team/f0ce0d89-bf39-46c6-8c42-28138d161321