FDA inspection
Trimedyne Inc: FDA inspection ending Jul 22, 2011
FDA inspection 735632 · Voluntary Action Indicated (VAI) · Corona, CA
Key facts
| Inspection ID | 735632 |
|---|---|
| Firm | Trimedyne Inc |
| FEI number | 1419951 |
| Address | 519 N Smith Ave Ste 105 |
| City | Corona |
| State | CA |
| ZIP | 92878 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Jul 22, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Radiation Control and Health Safety Act |
| 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