# InterX Technologies, Richardson, TX – FDA Inspections

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

> Inspection records and compliance data for InterX Technologies in Richardson, Texas. 5 FDA inspections on record, last inspected July 25, 2025.

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## Details

- Name: InterX Technologies
- FEI Number: 3004786509
- Address Line 1: 870 N Dorothy Dr Ste 708
- City: Richardson
- State: Texas
- Zip Code: 75081
- Country Name: United States
- Address: 870 N Dorothy Dr Ste 708, Richardson, Texas 75081, United States
- Country: United States

## Related Documents

- FDA Inspection 1277086 - InterX Technologies - 2025-07-25 — source: FDA, date: July 25, 2025
- FDA Inspection 1277086 - InterX Technologies - 2025-07-25 — classification: No Action Indicated (NAI), source: FDA, date: July 25, 2025
- FDA Inspection 1277086 - InterX Technologies - 2025-07-25 — classification: No Action Indicated (NAI), source: FDA, date: July 25, 2025
- FDA Inspection 1192346 - InterX Technologies - 2022-11-22 — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2022
- FDA Inspection 1192346 - InterX Technologies - 2022-11-22 — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2022
- FDA Inspection 1120592 - InterX Technologies - 2020-02-13 — classification: No Action Indicated (NAI), source: FDA, date: February 13, 2020
- FDA Inspection 1120592 - InterX Technologies - 2020-02-13 — classification: No Action Indicated (NAI), source: FDA, date: February 13, 2020
- FDA Inspection 975150 - InterX Technologies - 2016-06-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 3, 2016
- [FDA Inspection 975150 - InterX Technologies - 2016-06-03](https://www.keypedia.com/records/fda_inspections/interx-technologies/f8d5fb64-7a65-4638-8668-da90a5d59677) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 3, 2016
- FDA Inspection 760495 - InterX Technologies - 2012-01-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 5, 2012

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