FDA inspection
ANTEIS SA: FDA inspection ending Feb 27, 2026
FDA inspection 1307162 · No Action Indicated (NAI) · Lonay
Key facts
| Inspection ID | 1307162 |
|---|---|
| Firm | ANTEIS SA |
| FEI number | 3015471896 |
| Address | Chemin D' Etraz 2 |
| City | Lonay |
| Fiscal year | 2026 |
| Inspection end date | Feb 27, 2026 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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