FDA inspection
EONE Laboratories: FDA inspection ending Sep 23, 2025
FDA inspection 1294048 · No Action Indicated (NAI) · Yeonsu District
Key facts
| Inspection ID | 1294048 |
|---|---|
| Firm | EONE Laboratories |
| FEI number | 3012094568 |
| Address | 291 Harmony-Ro |
| City | Yeonsu District |
| Country | Korea (the Republic of) |
| Fiscal year | 2025 |
| Inspection end date | Sep 23, 2025 |
| Classification | No Action Indicated (NAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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