# OMNIA, Inc. – FDA Inspection, Mar 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/omnia-inc/f75e2d77-65cf-4d74-930e-6c996208568b
Source feed: FDA_Inspections

> FDA inspection 1007422 of OMNIA, Inc., March 28, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1007422
- Company Name: OMNIA, Inc.
- Inspection Date: 2017-03-28
- 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: 2

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

Company: https://www.keypedia.com/companies/omnia-inc/2d4fc955-f8ee-4ffc-ac2e-067f746ed3fa

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