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FDA Inspection 900399 — Myriad Genetics Laboratories, Inc.

Myriad Genetics Laboratories, Inc. — FEI 3030654068

The FDA completed an inspection of Myriad Genetics Laboratories, Inc. on October 10, 2014 in Salt Lake City, UT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 10, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Salt Lake City, UT (United States)

Facility

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FDA data resources