Myriad Genetics Laboratories, Inc.

Form 483FOIA Uncovered

Salt Lake City, Utah, United StatesFEI 3030654068Issued March 28, 2019

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3030654068.

Observations2

Issue DateMarch 28, 2019

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Myriad Genetics Laboratories, Inc.
Location: Salt Lake City, Utah, United States
FEI Number: 3030654068
Product Type: Devices
Issue Date: March 28, 2019
Country: United States

Inspection History, 2014 to 2024

NAI3

VAI3

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Myriad Genetics Laboratories, Inc. FDA Form 483, Salt Lake City, Utah, March 28, 2019