FDA inspection
Viper Technologies, LLC dba Avalign Thortex: FDA inspection ending Aug 26, 2004
FDA inspection 344519 · Voluntary Action Indicated (VAI) · Portland, OR
Key facts
| Inspection ID | 344519 |
|---|---|
| Firm | Viper Technologies, LLC dba Avalign Thortex |
| FEI number | 1000135253 |
| Address | 15045 Ne Mason St |
| City | Portland |
| State | OR |
| ZIP | 97230-4357 |
| Fiscal year | 2004 |
| Inspection end date | Aug 26, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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