# FDA Inspection 630668 - Ortheon Medical - November 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/ortheon-medical/29ccd302-231d-4a4a-959e-bf276f5658df
Source feed: FDA_Inspections

> FDA Inspection 630668 for Ortheon Medical on November 30, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 630668
- Company Name: Ortheon Medical
- Inspection Date: 2009-11-30
- 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.keypedia.com/companies/ortheon-medical/9e1949d8-b731-482f-b041-b3aa85716262

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