Gulbrandsen Technologies
United States Updated 9 July 2026
Gulbrandsen Technologies is an API manufacturer based in United States. It holds one active US drug master file. Its most recent recorded inspection, by US FDA, closed on 16 February 2022 as VAI.
1
registered plants
1 with an FDA FEI number
0
filings
across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Inspections
2 of 2 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.
Inspection history
- 16 February 2022 VAI US FDA
- 26 August 2015 VAI US FDA
NAI means no action indicated, VAI means voluntary action indicated, and OAI means
official action indicated.
Registered plants
| Site | FDA FEI |
| Orangeburg, United States | 1000111095 |
What they file, and where
Also appears on these molecule pages
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Open risk flags
- The most recent inspection outcome was VAI, on 16 February 2022.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability