FDA inspection
NeuroVention, LLC: FDA inspection ending May 31, 2023
FDA inspection 1206678 · Voluntary Action Indicated (VAI) · Daytona Beach, FL
Key facts
| Inspection ID | 1206678 |
|---|---|
| Firm | NeuroVention, LLC |
| FEI number | 3017884860 |
| Address | 645 S Beach St |
| City | Daytona Beach |
| State | FL |
| ZIP | 32114 |
| Country | United States |
| Fiscal year | 2023 |
| Inspection end date | May 31, 2023 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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