FDA inspection
Dilon Medical Technologies Inc.: FDA inspection ending Nov 19, 2013
FDA inspection 857250 · No Action Indicated (NAI) · Newport News, VA
Key facts
| Inspection ID | 857250 |
|---|---|
| Firm | Dilon Medical Technologies Inc. |
| FEI number | 3010060126 |
| Address | 6120 Windward Pkwy Ste 160 |
| City | Newport News |
| State | VA |
| ZIP | 23606 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Nov 19, 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