FDA inspection
Aretech, LLC: FDA inspection ending Jul 17, 2015
FDA inspection 935803 · Voluntary Action Indicated (VAI) · Ashburn, VA
Key facts
| Inspection ID | 935803 |
|---|---|
| Firm | Aretech, LLC |
| FEI number | 3007797030 |
| Address | 21720 Red Rum Dr Ste 187 |
| City | Ashburn |
| State | VA |
| ZIP | 20147 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Jul 17, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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