FDA inspection
Henogen SRL: FDA inspection ending Nov 22, 2024
FDA inspection 1254773 · Voluntary Action Indicated (VAI) · Seneffe
Key facts
| Inspection ID | 1254773 |
|---|---|
| Firm | Henogen SRL |
| FEI number | 3005932318 |
| Address | Rue De La Marlette 14 |
| City | Seneffe |
| Country | Belgium |
| Fiscal year | 2025 |
| Inspection end date | Nov 22, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
At a glance
- None Citations
- 1–9 Posted citations
- No 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