Time Cap Laboratories
United States 73 employees Updated 9 July 2026
Time Cap Laboratories is a finished-dose manufacturer based in United States. It appears in 10 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with US FDA and Health Canada. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 24 April 2025 as VAI.
1
registered plants
1 with an FDA FEI number
10
filings
across 2 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
- 24 April 2025 VAI US FDA
- 18 December 2019 VAI US FDA
- 12 March 2018 VAI US FDA
- 10 March 2016 VAI US FDA
- 16 January 2015 VAI US FDA
- 25 October 2013 NAI US FDA
- 18 March 2013 VAI US FDA
- 18 November 2011 VAI US FDA
NAI means no action indicated, VAI means voluntary action indicated, and OAI means
official action indicated.
Registered plants
| Site | FDA FEI |
| FARMINGDALE, United States | 2431898 |
Filings and GMP by regulator
| Regulator | Filings | GMP certificates |
| US FDA | 9 | 1 |
| Health Canada | 1 | None |
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Open risk flags
- The most recent inspection outcome was VAI, on 24 April 2025.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates