# Lutonix Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/lutonix-inc/0735c325-1f2e-408b-b289-2b13595f1e15

> Inspection records and compliance data for Lutonix Inc. in Tempe, Arizona. Access full analysis and detailed observations.

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## Details

- Name: Lutonix Inc.
- FEI Number: 3006513822
- City: Tempe
- State: Arizona
- Country Name: United States
- Address Line 1: 1625 W 3rd St
- Zip Code: 85281

## Related Documents

- [FDA Inspection 1077874 - Lutonix Inc. - 2019-01-25](https://www.globalkeysolutions.net/records/fda_inspections/lutonix-inc/316b90c0-1f80-4c76-960f-13e728d0e195) — classification: No Action Indicated (NAI), source: FDA, date: January 25, 2019
- [FDA Inspection 1077874 - Lutonix Inc. - 2019-01-25](https://www.globalkeysolutions.net/records/fda_inspections/lutonix-inc/fe1902d0-2712-4de8-b4ee-4b5449143bbc) — classification: No Action Indicated (NAI), source: FDA, date: January 25, 2019
- [FDA Inspection 1014338 - Lutonix Inc. - 2017-05-24](https://www.globalkeysolutions.net/records/fda_inspections/lutonix-inc/6c5868cf-b556-49e5-a560-2426d3cc3162) — classification: No Action Indicated (NAI), source: FDA, date: May 24, 2017
- [FDA Inspection 953355 - Lutonix Inc. - 2015-12-17](https://www.globalkeysolutions.net/records/fda_inspections/lutonix-inc/4106547e-7de3-446b-8ba8-5efd82ce520d) — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2015
- [FDA Inspection 953355 - Lutonix Inc. - 2015-12-17](https://www.globalkeysolutions.net/records/fda_inspections/lutonix-inc/df0fb2ca-0d47-4118-b2c1-2e3fda0a4a9e) — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2015
- [FDA Inspection 862326 - Lutonix Inc. - 2014-01-15](https://www.globalkeysolutions.net/records/fda_inspections/lutonix-inc/6b79989c-4565-4406-bbb9-ad2bc75dd591) — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2014
- [FDA Inspection 838849 - Lutonix Inc. - 2013-06-25](https://www.globalkeysolutions.net/records/fda_inspections/lutonix-inc/5f719fdd-d11a-4914-90aa-6bef8a51919f) — classification: No Action Indicated (NAI), source: FDA, date: June 25, 2013

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