Ohm Laboratories
United States 27 employees Updated 9 July 2026
Ohm Laboratories is a finished-dose manufacturer based in United States. It appears in 16 regulatory filings 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 31 October 2024 as NAI.
1
registered plants
1 with an FDA FEI number
16
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
- 31 October 2024 NAI US FDA
- 12 January 2024 NAI US FDA
- 10 November 2022 NAI US FDA
- 2 August 2021 NAI US FDA
- 5 February 2020 VAI US FDA
- 17 August 2018 NAI US FDA
- 8 November 2017 NAI US FDA
- 22 November 2016 NAI US FDA
NAI means no action indicated, VAI means voluntary action indicated, and OAI means
official action indicated.
Registered plants
| Site | FDA FEI |
| North Brunswick, United States | 3004132058 |
Filings and GMP by regulator
| Regulator | Filings | GMP certificates |
| US FDA | 16 | 1 |
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Open risk flags
- The most recent inspection outcome was NAI, on 31 October 2024.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates