# FDA Inspection 805363 - Abeon Medical Corporation - October 30, 2012

Source: https://www.keypedia.com/records/fda_inspections/abeon-medical-corporation/1ecfbd2f-38b5-4f03-962e-304eefe682d3
Source feed: FDA_Inspections

> FDA Inspection 805363 for Abeon Medical Corporation on October 30, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 805363
- Company Name: Abeon Medical Corporation
- Inspection Date: 2012-10-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 805363 - 2012-10-30](https://www.keypedia.com/records/fda_inspections/abeon-medical-corporation/409aa25c-8725-41a5-9793-556490495fd2)

Company: https://www.keypedia.com/companies/abeon-medical-corporation/c7ca4675-2b59-4388-9669-a757f4f4f4b6

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