Pisgah Laboratories
United States Updated 9 July 2026
Pisgah Laboratories 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 21 October 2021 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
4 of 4 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.
Inspection history
- 21 October 2021 VAI US FDA
- 8 April 2016 VAI US FDA
- 1 August 2012 NAI US FDA
- 8 July 2009 NAI US FDA
NAI means no action indicated, VAI means voluntary action indicated, and OAI means
official action indicated.
Registered plants
| Site | FDA FEI |
| Pisgah Forest, United States | 3001237833 |
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 21 October 2021.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability