# iMed Technology, Inc - Inspection Records

Source: https://www.keypedia.com/companies/imed-technology-inc/08272093-861d-4968-a375-dd65280700e4

> Inspection records and compliance data for iMed Technology, Inc in Carrollton, Texas. Access full analysis and detailed observations.

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## Details

- Name: iMed Technology, Inc
- FEI Number: 3003813437
- City: Carrollton
- State: Texas
- Country Name: United States
- Address Line 1: 3235 Skylane Dr Ste 127
- Zip Code: 75006

## Related Documents

- [FDA Inspection 1279425 - iMed Technology, Inc - 2025-08-06](https://www.keypedia.com/records/fda_inspections/imed-technology-inc/2464eac9-dedd-4f89-9b65-bc86bbd5dec3) — source: FDA, date: August 6, 2025
- [FDA Inspection 1279425 - iMed Technology, Inc - 2025-08-06](https://www.keypedia.com/records/fda_inspections/imed-technology-inc/b88a05c3-3c98-46b8-9006-998cddf8269c) — classification: No Action Indicated (NAI), source: FDA, date: August 6, 2025
- [483 - iMed Technology, Inc - 2022-10-18](https://www.keypedia.com/records/483/imed-technology-inc/83ec2e2e-85bf-4623-b8f0-14f8de5b8276) — source: FDA, date: October 18, 2022
- [FDA Inspection 1181689 - iMed Technology, Inc - 2022-10-18](https://www.keypedia.com/records/fda_inspections/imed-technology-inc/0e6d9fc4-4933-4891-9e36-84a499e18495) — classification: No Action Indicated (NAI), source: FDA, date: October 18, 2022
- [FDA Inspection 1181689 - iMed Technology, Inc - 2022-10-18](https://www.keypedia.com/records/fda_inspections/imed-technology-inc/75d3827b-0b84-43d7-9304-3669117a0e22) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 18, 2022
- [FDA Inspection 1014455 - iMed Technology, Inc - 2017-06-16](https://www.keypedia.com/records/fda_inspections/imed-technology-inc/ca0f9f28-cb1f-4117-b0dc-9145bc5039cb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 16, 2017
- [FDA Inspection 1014455 - iMed Technology, Inc - 2017-06-16](https://www.keypedia.com/records/fda_inspections/imed-technology-inc/f149f8a2-6764-41af-8852-bcfa874c33ba) — classification: No Action Indicated (NAI), source: FDA, date: June 16, 2017
- [FDA Inspection 817134 - iMed Technology, Inc - 2013-01-30](https://www.keypedia.com/records/fda_inspections/imed-technology-inc/06cd4ac4-13c2-4435-9efe-6f7a6d31024e) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2013
- [FDA Inspection 817134 - iMed Technology, Inc - 2013-01-30](https://www.keypedia.com/records/fda_inspections/imed-technology-inc/981bab38-3512-424a-a0bd-8d59faeb3a9f) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2013
- [FDA Inspection 756359 - iMed Technology, Inc - 2011-12-08](https://www.keypedia.com/records/fda_inspections/imed-technology-inc/27dcce11-6b78-4275-b4b9-2005faba45f0) — classification: Official Action Indicated (OAI), source: FDA, date: December 8, 2011
- [FDA Inspection 756359 - iMed Technology, Inc - 2011-12-08](https://www.keypedia.com/records/fda_inspections/imed-technology-inc/281a91e9-f046-4684-90f2-df9c149283e5) — classification: Official Action Indicated (OAI), source: FDA, date: December 8, 2011

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