FDA inspection
The Snore Reliever Company LLC: FDA inspection ending Feb 5, 2020
FDA inspection 1116928 · Voluntary Action Indicated (VAI) · Largo, FL
Key facts
| Inspection ID | 1116928 |
|---|---|
| Firm | The Snore Reliever Company LLC |
| FEI number | 3008583502 |
| Address | 4201 Tonnelle Ave Ste 202 |
| City | Largo |
| State | FL |
| ZIP | 33773 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Feb 5, 2020 |
| 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