FDA Inspection 1277478 — GenoGenix LLC

GenoGenix LLC — FEI 3032144832

The FDA completed an inspection of GenoGenix LLC on Jul 18, 2025 in Boca Raton, FL. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Jul 18, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Boca Raton, FL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.