# FDA Inspection 1120592 - InterX Technologies - February 13, 2020

Source: https://www.keypedia.com/records/fda_inspections/interx-technologies/84eb8d6f-50d7-4929-984d-287ba92e6c8e
Source feed: FDA_Inspections

> FDA Inspection 1120592 for InterX Technologies on February 13, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1120592
- Company Name: InterX Technologies
- Inspection Date: 2020-02-13
- Classification: No Action Indicated (NAI)
- 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