FDA inspection
Bunnell, Inc.: FDA inspection ending Nov 3, 2017
FDA inspection 1042614 · Voluntary Action Indicated (VAI) · Salt Lake City, UT
Key facts
| Inspection ID | 1042614 |
|---|---|
| Firm | Bunnell, Inc. |
| FEI number | 1719232 |
| Address | 436 W Lawndale Dr |
| City | Salt Lake City |
| State | UT |
| ZIP | 84115-2917 |
| Fiscal year | 2018 |
| Inspection end date | Nov 3, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None 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