# Genia Medical, Inc. – FDA Inspection, Apr 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/genia-medical-inc/c9073e49-4077-4032-a501-9664cf5e0305
Source feed: FDA_Inspections

> FDA inspection 1012875 of Genia Medical, Inc., April 17, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1012875
- Company Name: Genia Medical, Inc.
- Inspection Date: 2017-04-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1233376 - 2024-02-15](https://www.keypedia.com/records/fda_inspections/genia-medical-inc/f5784b79-2730-40bd-9c54-4a16015e0794)

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

Company: https://www.keypedia.com/companies/genia-medical-inc/8c6d19e9-ea1d-4a34-a35c-f4adbb230243

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