# FDA Inspection 818494 - Aktina Medical Corp - February 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/aktina-medical-corp/6ea2e114-ecad-4551-887a-0f6f9b31db77
Source feed: FDA_Inspections

> FDA Inspection 818494 for Aktina Medical Corp on February 12, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 818494
- Company Name: Aktina Medical Corp
- Inspection Date: 2013-02-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 818494 - 2013-02-12](https://www.keypedia.com/records/fda_inspections/aktina-medical-corp/6905d71f-1457-4695-8518-1ba870560644)
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Company: https://www.keypedia.com/companies/aktina-medical-corp/d78d799a-6e65-4b26-825a-766d98946ebb

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