FDA inspection
Cura medical Technologies, LLC: FDA inspection ending Dec 11, 2015
FDA inspection 952103 · Voluntary Action Indicated (VAI) · Lake Forest, CA
Key facts
| Inspection ID | 952103 |
|---|---|
| Firm | Cura medical Technologies, LLC |
| FEI number | 3010768635 |
| Address | 23 Rancho Cir Ste B |
| City | Lake Forest |
| State | CA |
| ZIP | 92630 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Dec 11, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- None 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