# InterX Technologies – FDA Inspection, Jun 3, 2016

Source: https://www.keypedia.com/records/fda_inspections/interx-technologies/f8d5fb64-7a65-4638-8668-da90a5d59677
Source feed: FDA_Inspections

> FDA inspection 975150 of InterX Technologies, June 03, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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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