# FDA Inspection 1082466 - Omnia Medical - February 06, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/omnia-medical/5fa1f90d-93fa-4b17-b4b6-6f39237fec95
Source feed: FDA_Inspections

> FDA Inspection 1082466 for Omnia Medical on February 06, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1082466
- Company Name: Omnia Medical
- Inspection Date: 2019-02-06
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/omnia-medical/231109bd-5403-4992-861c-72049445d381

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