FDA Inspection 953260 — Myriad Genetics Laboratories, Inc.

Myriad Genetics Laboratories, Inc. — FEI 3030654068

The FDA completed an inspection of Myriad Genetics Laboratories, Inc. on Dec 4, 2015 in Salt Lake City, UT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 4, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Salt Lake City, UT (United States)

Additional details

Postmarket Audit Inspections

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