FDA Inspection 899814 — Myriad Genetics Laboratories, Inc.

Myriad Genetics Laboratories, Inc. — FEI 3030654068

The FDA completed an inspection of Myriad Genetics Laboratories, Inc. on Oct 17, 2014 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
Oct 17, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Salt Lake City, UT (United States)

Additional details

Clinical Investigator (CI)

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