# Genova Diagnostics – FDA Inspection, Feb 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/genova-diagnostics/b084704a-92f4-4b6e-9361-cc77c356006c
Source feed: FDA_Inspections

> FDA inspection 1009292 of Genova Diagnostics, February 24, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1009292
- Company Name: Genova Diagnostics
- Inspection Date: 2017-02-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Officers

- [Investigator](https://www.keypedia.com/people/christopher-b-may/b2173a59-d37b-41f1-aa39-eefd854722b8)
- [Issuing Officer](https://www.keypedia.com/people/trang-n-cox/436825b5-0375-4191-81b9-6e18b90d33af)

Company: https://www.keypedia.com/companies/genova-diagnostics/9d90aa38-ff52-4e7d-9f37-10b720ba15af

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