FDA inspection
Dune Medical Devices, Ltd: FDA inspection ending Apr 24, 2012
FDA inspection 783565 · No Action Indicated (NAI) · Caesarea
Key facts
| Inspection ID | 783565 |
|---|---|
| Firm | Dune Medical Devices, Ltd |
| FEI number | 3005755031 |
| Address | 20, Alon ha-Tavor |
| City | Caesarea |
| Country | Israel |
| Fiscal year | 2012 |
| Inspection end date | Apr 24, 2012 |
| 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