# Myriad Genetics Laboratories, Inc. – FDA Inspection, Mar 28, 2019

Source: https://www.keypedia.com/records/fda_inspections/myriad-genetics-laboratories-inc/73775860-ed57-46c9-8d18-b0d95fdc6d2a
Source feed: FDA_Inspections

> FDA inspection 1084183 of Myriad Genetics Laboratories, Inc., March 28, 2019. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1084183
- Company Name: Myriad Genetics Laboratories, Inc.
- Inspection Date: 2019-03-28
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1248251 - 2024-08-23

## Related Officers

- [Company Rep](https://www.keypedia.com/people/christine-i-shaw/480cb61e-f173-432d-b84a-c8b492192302)

Company: https://www.keypedia.com/companies/myriad-genetics-laboratories-inc/56f057d0-d9e3-4e5c-a697-d6dffa534653

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7