FDA inspection
MediView XR Inc.: FDA inspection ending Aug 26, 2025
FDA inspection 1280195 · No Action Indicated (NAI) · Cleveland, OH
Key facts
| Inspection ID | 1280195 |
|---|---|
| Firm | MediView XR Inc. |
| FEI number | 3016110967 |
| Address | 10000 Cedar Ave Ste Gcic2-153 |
| City | Cleveland |
| State | OH |
| ZIP | 44106 |
| Country | United States |
| Fiscal year | 2025 |
| Inspection end date | Aug 26, 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