FDA Inspection 1248251 — Myriad Genetics Laboratories, Inc.

Myriad Genetics Laboratories, Inc. — FEI 3030654068

The FDA completed an inspection of Myriad Genetics Laboratories, Inc. on Aug 23, 2024 in Salt Lake City, UT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 23, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Salt Lake City, UT (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.