FDA inspection
Nova-Vent Rx, Inc: FDA inspection ending Aug 18, 2004
FDA inspection 369645 · No Action Indicated (NAI) · Elk Grove Village, IL
Key facts
| Inspection ID | 369645 |
|---|---|
| Firm | Nova-Vent Rx, Inc |
| FEI number | 1420018 |
| Address | 106 N Lively Blvd |
| City | Elk Grove Village |
| State | IL |
| ZIP | 60007-1318 |
| Fiscal year | 2004 |
| Inspection end date | Aug 18, 2004 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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