# FDA Inspection 975150 - InterX Technologies - June 03, 2016

Source: https://www.keypedia.com/records/fda_inspections/interx-technologies/c3315d95-7b51-4cae-ba31-935d34deb38f
Source feed: FDA_Inspections

> FDA Inspection 975150 for InterX Technologies on June 03, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 975150
- Company Name: InterX Technologies
- Inspection Date: 2016-06-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/interx-technologies/e1f3e816-5173-4f0e-9228-b8d561253963

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