FDA inspection
Primus Corporation: FDA inspection ending Apr 15, 2009
FDA inspection 578776 · Voluntary Action Indicated (VAI) · Kansas City, MO
Key facts
| Inspection ID | 578776 |
|---|---|
| Firm | Primus Corporation |
| FEI number | 1931251 |
| Address | 4231 E 75th Ter |
| City | Kansas City |
| State | MO |
| ZIP | 64132 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Apr 15, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| 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
- 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