FDA inspection
ARUP Laboratories, Inc.: FDA inspection ending Nov 18, 2016
FDA inspection 998801 · Voluntary Action Indicated (VAI) · Salt Lake City, UT
Key facts
| Inspection ID | 998801 |
|---|---|
| Firm | ARUP Laboratories, Inc. |
| FEI number | 3004741920 |
| Address | 565 S Komas Dr |
| City | Salt Lake City |
| State | UT |
| ZIP | 84108 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Nov 18, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
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
- 10–99 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