FDA inspection
Nuvonyx: FDA inspection ending Feb 28, 2000
FDA inspection 16024 · Voluntary Action Indicated (VAI) · Bridgeton, MO
Key facts
| Inspection ID | 16024 |
|---|---|
| Firm | Nuvonyx |
| FEI number | 3002942292 |
| Address | 3753 Pennridge Dr |
| City | Bridgeton |
| State | MO |
| ZIP | 63044-1226 |
| Fiscal year | 2000 |
| Inspection end date | Feb 28, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| 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