Suppliers / Cenexi - Laboratoires Thissen S. A
Cenexi - Laboratoires Thissen S. A
Belgium Updated 9 July 2026
Cenexi - Laboratoires Thissen S. A is a finished-dose manufacturer based in Belgium. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by ANVISA (Brazil), MFDS (Korea) and US FDA. Its most recent recorded inspection, by US FDA, closed on 1 June 2023 as VAI.
2
registered plants
1 with an FDA FEI number
1
filings
across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.
Inspection history
- 1 June 2023 VAI US FDA
- 6 December 2022 VAI US FDA
- 19 February 2020 VAI US FDA
- 16 December 2016 VAI US FDA
- 18 June 2015 VAI US FDA
- 4 April 2014 NAI US FDA
- 17 July 2012 VAI US FDA
- 11 February 2010 VAI US FDA
NAI means no action indicated, VAI means voluntary action indicated, and OAI means
official action indicated.
Registered plants
| Site | FDA FEI |
| WALLON BRABANT, Belgium | Not on file |
| Belgium, Belgium | 3007388138 |
Filings and GMP by regulator
| Regulator | Filings | GMP certificates |
| ARCSA (EC) | 1 | None |
| ANVISA (Brazil) | None | 3 |
| MFDS (Korea) | None | 2 |
| US FDA | None | 1 |
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Open risk flags
- The most recent inspection outcome was VAI, on 1 June 2023.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates