FDA inspection
Westone Laboratories, Inc.: FDA inspection ending Nov 15, 2017
FDA inspection 1031336 · Voluntary Action Indicated (VAI) · Colorado Springs, CO
Key facts
| Inspection ID | 1031336 |
|---|---|
| Firm | Westone Laboratories, Inc. |
| FEI number | 2094377 |
| Address | 2235 Executive Cir |
| City | Colorado Springs |
| State | CO |
| ZIP | 80906 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Nov 15, 2017 |
| 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