FDA inspection
GenoGenix LLC: FDA inspection ending Jul 18, 2025
FDA inspection 1277478 · Official Action Indicated (OAI) · Boca Raton, FL
Key facts
| Inspection ID | 1277478 |
|---|---|
| Firm | GenoGenix LLC |
| FEI number | 3032144832 |
| Address | 2840 Nw 2nd Ave Ste 204 |
| City | Boca Raton |
| State | FL |
| ZIP | 33431 |
| Country | United States |
| Fiscal year | 2025 |
| Inspection end date | Jul 18, 2025 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
| Warning letter | 718739 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data