Nantong Chanyoo Pharmatech
China Updated 9 July 2026
Nantong Chanyoo Pharmatech is an API manufacturer based in China. Its GMP standing is certified by MFDS (Korea) and US FDA. Its most recent recorded inspection, by US FDA, closed on 16 May 2025 as NAI.
1
registered plants
1 with an FDA FEI number
0
filings
across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Inspections
3 of 3 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.
Inspection history
- 16 May 2025 NAI US FDA
- 22 March 2019 VAI US FDA
- 18 September 2015 VAI US FDA
NAI means no action indicated, VAI means voluntary action indicated, and OAI means
official action indicated.
Registered plants
| Site | FDA FEI |
| China, China | 3011243688 |
What they file, and where
| Molecule | Regulators | Docs |
| Ezetimibe | SFDA (Saudi Arabia) | 1 |
| Rosuvastatin | SFDA (Saudi Arabia) | 1 |
| Sofosbuvir | SFDA (Saudi Arabia) | 1 |
| Ticagrelor | SFDA (Saudi Arabia) | 1 |
Also appears on these molecule pages
Filings and GMP by regulator
| Regulator | Filings | GMP certificates |
| MFDS (Korea) | None | 2 |
| US FDA | None | 1 |
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Open risk flags
- The most recent inspection outcome was NAI, on 16 May 2025.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates