FDA inspection
Katecho Inc: FDA inspection ending Nov 18, 2005
FDA inspection 404591 · Voluntary Action Indicated (VAI) · Des Moines, IA
Key facts
| Inspection ID | 404591 |
|---|---|
| Firm | Katecho Inc |
| FEI number | 1930027 |
| Address | 4020 Gannett Ave |
| City | Des Moines |
| State | IA |
| ZIP | 50321-2951 |
| Fiscal year | 2006 |
| Inspection end date | Nov 18, 2005 |
| 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