FDA inspection
Myriad Genetics Laboratories, Inc.: FDA inspection ending Aug 23, 2024
FDA inspection 1248251 · No Action Indicated (NAI) · Salt Lake City, UT
Key facts
| Inspection ID | 1248251 |
|---|---|
| Firm | Myriad Genetics Laboratories, Inc. |
| FEI number | 3030654068 |
| Address | 322 N 2200 W |
| City | Salt Lake City |
| State | UT |
| ZIP | 84116 |
| Country | United States |
| Fiscal year | 2024 |
| Inspection end date | Aug 23, 2024 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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