FDA inspection
Dynex Technologies, Inc.: FDA inspection ending Jul 9, 2002
FDA inspection 226236 · Chantilly, VA
Key facts
| Inspection ID | 226236 |
|---|---|
| Firm | Dynex Technologies, Inc. |
| FEI number | 1117676 |
| Address | 14340 Sullyfield Cir |
| City | Chantilly |
| State | VA |
| ZIP | 20151-1621 |
| Fiscal year | 2002 |
| Inspection end date | Jul 9, 2002 |
| Project area | Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| 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