FDA inspection
iMed Technology, Inc: FDA inspection ending Jan 30, 2013
FDA inspection 817134 · No Action Indicated (NAI) · Mckinney, TX
Key facts
| Inspection ID | 817134 |
|---|---|
| Firm | iMed Technology, Inc |
| FEI number | 3003813437 |
| Address | 3235 Skylane Dr Ste 127 |
| City | Mckinney |
| State | TX |
| ZIP | 75070 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Jan 30, 2013 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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