FDA inspection
Visura Technologies, Inc.: FDA inspection ending Mar 24, 2026
FDA inspection 1300774 · Voluntary Action Indicated (VAI) · Minneapolis, MN
Key facts
| Inspection ID | 1300774 |
|---|---|
| Firm | Visura Technologies, Inc. |
| FEI number | 3015194986 |
| Address | 8400 Normandale Lake Blvd Ste 920 |
| City | Minneapolis |
| State | MN |
| ZIP | 55437 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Mar 24, 2026 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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