FDA inspection
Rapid Reboot Recovery Products, LLC: FDA inspection ending Nov 29, 2018
FDA inspection 1073080 · Voluntary Action Indicated (VAI) · Lindon, UT
Key facts
| Inspection ID | 1073080 |
|---|---|
| Firm | Rapid Reboot Recovery Products, LLC |
| FEI number | 3013787796 |
| Address | 1396 W 200 S Bldg 2 Unit A |
| City | Lindon |
| State | UT |
| ZIP | 84042 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Nov 29, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| 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