FDA inspection
Kavo America Corporation: FDA inspection ending May 6, 2004
FDA inspection 333237 · No Action Indicated (NAI) · Lake Zurich, IL
Key facts
| Inspection ID | 333237 |
|---|---|
| Firm | Kavo America Corporation |
| FEI number | 1419798 |
| Address | 340 E Il Route 22 |
| City | Lake Zurich |
| State | IL |
| ZIP | 60047-2572 |
| Fiscal year | 2004 |
| Inspection end date | May 6, 2004 |
| Classification | No Action Indicated (NAI) |
| Project area | Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| Product type | Devices |
At a glance
- None Citations
- None 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