Cetylite Industries
United States 29 employees Updated 9 July 2026
Cetylite Industries is a finished-dose manufacturer based in United States. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 9 December 2024 as VAI.
1
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
- 9 December 2024 VAI US FDA
- 2 March 2023 OAI US FDA
- 24 September 2021 OAI US FDA
- 29 May 2018 VAI US FDA
- 19 November 2015 VAI US FDA
- 12 July 2013 VAI US FDA
- 26 April 2011 VAI US FDA
- 14 October 2008 NAI US FDA
NAI means no action indicated, VAI means voluntary action indicated, and OAI means
official action indicated.
Registered plants
| Site | FDA FEI |
| Pennsauken, United States | 2242327 |
Filings and GMP by regulator
| Regulator | Filings | GMP certificates |
| Health Canada | 1 | None |
| US FDA | None | 1 |
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Open risk flags
- The most recent inspection outcome was VAI, on 9 December 2024.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates