FDA inspection

Myriad Genetics Laboratories, Inc.: FDA inspection ending Mar 28, 2019

FDA inspection 1084183 · Voluntary Action Indicated (VAI) · Salt Lake City, UT

Key facts

Inspection ID 1084183
Firm Myriad Genetics Laboratories, Inc.
FEI number 3030654068
Address 320 S Wakara Way
City Salt Lake City
State UT
ZIP 84116
Country United States
Fiscal year 2019
Inspection end date Mar 28, 2019
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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