FDA inspection
Ekso Bionics: FDA inspection ending Jun 28, 2019
FDA inspection 1097120 · No Action Indicated (NAI) · San Rafael, CA
Key facts
| Inspection ID | 1097120 |
|---|---|
| Firm | Ekso Bionics |
| FEI number | 3009495988 |
| Address | 1414 Harbour Way S Ste 1201 |
| City | San Rafael |
| State | CA |
| ZIP | 94901 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Jun 28, 2019 |
| 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