FDA inspection
Xoran Technologies, LLC.: FDA inspection ending Dec 20, 2017
FDA inspection 1035619 · Voluntary Action Indicated (VAI) · Ann Arbor, MI
Key facts
| Inspection ID | 1035619 |
|---|---|
| Firm | Xoran Technologies, LLC. |
| FEI number | 3004198450 |
| Address | 5210 S State Rd |
| City | Ann Arbor |
| State | MI |
| ZIP | 48108 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Dec 20, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Radiation Control and Health Safety Act |
| Product type | Devices |
At a glance
- 1–9 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