# FDA Inspection 1007422 - OMNIA, Inc. - March 28, 2017

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

> FDA Inspection 1007422 for OMNIA, Inc. on March 28, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1007422 - 2017-03-28](https://www.globalkeysolutions.net/api/records/fda_inspections/omnia-inc/ddc69264-3224-4484-91af-c4f18410ce53/)

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

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