FDA inspection
TriMed Inc.: FDA inspection ending Mar 1, 2007
FDA inspection 461920 · Voluntary Action Indicated (VAI) · Santa Clarita, CA
Key facts
| Inspection ID | 461920 |
|---|---|
| Firm | TriMed Inc. |
| FEI number | 3001236812 |
| Address | 27533 Avenue Hopkins |
| City | Santa Clarita |
| State | CA |
| ZIP | 91355-3910 |
| Fiscal year | 2007 |
| Inspection end date | Mar 1, 2007 |
| 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
- 10–99 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