FDA Inspection 953260 — Myriad Genetics Laboratories, Inc.
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