# FDA Inspection 761092 - Aurident Inc - December 07, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/aurident-inc/f9e69607-b00e-4efa-a22c-9569dc77e579/
Source feed: FDA_Inspections

> FDA Inspection 761092 for Aurident Inc on December 07, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 761092
- Company Name: Aurident Inc
- Inspection Date: 2011-12-07
- 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/aurident-inc/498bd7dc-e80f-4ded-a3cf-4aef0103af22

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