FDA inspection
Hummingbird Med Devices, Inc.: FDA inspection ending Aug 26, 2019
FDA inspection 1100442 · Voluntary Action Indicated (VAI) · Camano Island, WA
Key facts
| Inspection ID | 1100442 |
|---|---|
| Firm | Hummingbird Med Devices, Inc. |
| FEI number | 3009382876 |
| Address | 1283 Elger Bay Rd Ste D |
| City | Camano Island |
| State | WA |
| ZIP | 98282 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Aug 26, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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