# FDA Inspection 812708 - Perseon Corporation - December 19, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/perseon-corporation/763aacf9-7d50-4e8b-bfaf-d2c8a63b5509/
Source feed: FDA_Inspections

> FDA Inspection 812708 for Perseon Corporation on December 19, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 812708
- Company Name: Perseon Corporation
- Inspection Date: 2012-12-19
- 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/perseon-corporation/2cf0833f-60e1-4a7f-9299-3b3a5d4e85e8

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