FDA inspection
InterX Technologies: FDA inspection ending Sep 20, 2006
FDA inspection 452707 · Richardson, TX
Key facts
| Inspection ID | 452707 |
|---|---|
| Firm | InterX Technologies |
| FEI number | 3004786509 |
| Address | 870 N Dorothy Dr Ste 708 |
| City | Richardson |
| State | TX |
| ZIP | 75081-2771 |
| Fiscal year | 2006 |
| Inspection end date | Sep 20, 2006 |
| 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