Central Glass Co.,Ltd
Japan Updated 9 July 2026
Central Glass Co.,Ltd is an API manufacturer based in Japan. It holds 2 active US drug master files. Its filings concentrate with EEC_EAEU and NCELS (KZ). Its GMP standing is certified by ZLG (DE) and US FDA. Its most recent recorded inspection, by US FDA, closed on 15 September 2023 as VAI.
2
registered plants
1 with an FDA FEI number
9
filings
across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
Inspections
5 of 5 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.
Inspection history
- 15 September 2023 VAI US FDA
- 29 June 2018 VAI US FDA
- 19 September 2014 VAI US FDA
- 9 February 2012 VAI US FDA
- 24 July 2009 VAI US FDA
NAI means no action indicated, VAI means voluntary action indicated, and OAI means
official action indicated.
Registered plants
| Site | FDA FEI |
| Halle-Kuensebeck, Germany | Not on file |
| Japan, Japan | 3002806649 |
What they file, and where
Also appears on these molecule pages
Filings and GMP by regulator
| Regulator | Filings | GMP certificates |
| EEC_EAEU | 8 | None |
| NCELS (KZ) | 1 | None |
| ZLG (DE) | None | 2 |
| US FDA | None | 1 |
Comparing suppliers?
Choose your molecules and target markets. Central Glass Co.,Ltd comes back tiered against every other
supplier able to file there.
Start for free No sales call.
Open risk flags
- The most recent inspection outcome was VAI, on 15 September 2023.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates