FDA inspection
OXITONE MEDICAL LTD: FDA inspection ending Jun 15, 2023
FDA inspection 1208818 · Voluntary Action Indicated (VAI) · Kfar Saba
Key facts
| Inspection ID | 1208818 |
|---|---|
| Firm | OXITONE MEDICAL LTD |
| FEI number | 3015143060 |
| Address | 17, Atir Yeda |
| City | Kfar Saba |
| Country | Israel |
| Fiscal year | 2023 |
| Inspection end date | Jun 15, 2023 |
| 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