FDA inspection
Rehabtronics Inc.: FDA inspection ending Feb 26, 2015
FDA inspection 916001 · Official Action Indicated (OAI) · Edmonton
Key facts
| Inspection ID | 916001 |
|---|---|
| Firm | Rehabtronics Inc. |
| FEI number | 3007999109 |
| Address | 4352-10230 Jasper Ave Nw |
| City | Edmonton |
| Country | Canada |
| Fiscal year | 2015 |
| Inspection end date | Feb 26, 2015 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 10–99 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