# InterX Technologies - Inspection Records

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

> Inspection records and compliance data for InterX Technologies in Richardson, Texas. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1277086 - InterX Technologies - 2025-07-25](https://www.keypedia.com/records/fda_inspections/interx-technologies/61a96d7c-4038-4120-ae70-fad694421d5b) — source: FDA, date: July 25, 2025
- [FDA Inspection 1277086 - InterX Technologies - 2025-07-25](https://www.keypedia.com/records/fda_inspections/interx-technologies/37fdb161-879d-402c-bf72-0dcd02ce2b85) — classification: No Action Indicated (NAI), source: FDA, date: July 25, 2025
- [FDA Inspection 1277086 - InterX Technologies - 2025-07-25](https://www.keypedia.com/records/fda_inspections/interx-technologies/2fb3715f-1b9d-4e6a-aeec-7ef6294650da) — classification: No Action Indicated (NAI), source: FDA, date: July 25, 2025
- [FDA Inspection 1192346 - InterX Technologies - 2022-11-22](https://www.keypedia.com/records/fda_inspections/interx-technologies/9408f015-803b-44c6-9c2a-eeb0f4bbc0fc) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2022
- [FDA Inspection 1192346 - InterX Technologies - 2022-11-22](https://www.keypedia.com/records/fda_inspections/interx-technologies/8ea33022-7c8c-4e8b-a30f-01a6bc4471c8) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2022
- [FDA Inspection 1120592 - InterX Technologies - 2020-02-13](https://www.keypedia.com/records/fda_inspections/interx-technologies/84eb8d6f-50d7-4929-984d-287ba92e6c8e) — classification: No Action Indicated (NAI), source: FDA, date: February 13, 2020
- [FDA Inspection 1120592 - InterX Technologies - 2020-02-13](https://www.keypedia.com/records/fda_inspections/interx-technologies/20fcabab-5ee1-4a86-a596-60c1b0a40b22) — classification: No Action Indicated (NAI), source: FDA, date: February 13, 2020
- [FDA Inspection 975150 - InterX Technologies - 2016-06-03](https://www.keypedia.com/records/fda_inspections/interx-technologies/c3315d95-7b51-4cae-ba31-935d34deb38f) — 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](https://www.keypedia.com/records/fda_inspections/interx-technologies/54b7d1e9-8ce1-472a-875d-8d6c2df195b5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 5, 2012

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