FDA inspection
Sonablate Corp.: FDA inspection ending Nov 29, 2017
FDA inspection 1032390 · Voluntary Action Indicated (VAI) · Charlotte, NC
Key facts
| Inspection ID | 1032390 |
|---|---|
| Firm | Sonablate Corp. |
| FEI number | 3007126306 |
| Address | 10130 Perimeter Pkwy Ste 250 |
| City | Charlotte |
| State | NC |
| ZIP | 28216 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Nov 29, 2017 |
| 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