# FDA Inspection 760495 - InterX Technologies - January 05, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/interx-technologies/db7964ed-4d54-4d64-8b8e-370fe331ea23
Source feed: FDA_Inspections

> FDA Inspection 760495 for InterX Technologies on January 05, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 760495
- Company Name: InterX Technologies
- Inspection Date: 2012-01-05
- 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/interx-technologies/e1f3e816-5173-4f0e-9228-b8d561253963

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