FDA inspection
LISI MEDICAL FASTENERS: FDA inspection ending Apr 16, 2025
FDA inspection 1269118 · No Action Indicated (NAI) · Neyron
Key facts
| Inspection ID | 1269118 |
|---|---|
| Firm | LISI MEDICAL FASTENERS |
| FEI number | 3003690049 |
| Address | 19 Chemin De La Traille, B.P. 100 |
| City | Neyron |
| Country | France |
| Fiscal year | 2025 |
| Inspection end date | Apr 16, 2025 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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