FDA inspection
ARUP Laboratories Inc.: FDA inspection ending Mar 14, 2019
FDA inspection 1087820 · Voluntary Action Indicated (VAI) · Salt Lake City, UT
Key facts
| Inspection ID | 1087820 |
|---|---|
| Firm | ARUP Laboratories Inc. |
| FEI number | 3008974012 |
| Address | 50 N Medical Dr Rm A610 |
| City | Salt Lake City |
| State | UT |
| ZIP | 84132 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Mar 14, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
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