FDA inspection
Dilon Technologies Inc: FDA inspection ending Sep 27, 2019
FDA inspection 1123477 · Voluntary Action Indicated (VAI) · Newport News, VA
Key facts
| Inspection ID | 1123477 |
|---|---|
| Firm | Dilon Technologies Inc |
| FEI number | 3002931663 |
| Address | 12050 Jefferson Ave Ste 340 |
| City | Newport News |
| State | VA |
| ZIP | 23606-4471 |
| Fiscal year | 2019 |
| Inspection end date | Sep 27, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| 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