# Lightwave - Inspection Records

Source: https://www.globalkeysolutions.net/companies/lightwave/ab86405c-ae8f-4ab3-b9ae-dc51352e9a61

> Inspection records and compliance data for Lightwave in Phoenix, Arizona. Access full analysis and detailed observations.

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## Details

- Name: Lightwave
- FEI Number: 3009241253
- City: Phoenix
- State: Arizona
- Country Name: United States
- Address Line 1: 2205 W Lone Cactus Dr Ste 11
- Zip Code: 85027

## Related Documents

- [483 - Lightwave - 2025-10-22](https://www.globalkeysolutions.net/records/483/lightwave/182f38cc-2bf5-4429-b3ac-0cb4bf449a21) — source: FDA, date: October 22, 2025
- [FDA Inspection 1291402 - Lightwave - 2025-10-22](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/cbc2c446-e7cd-4410-9cb5-fe0399908836) — classification: Official Action Indicated (OAI), source: FDA, date: October 22, 2025
- [FDA Inspection 1291402 - Lightwave - 2025-10-22](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/2996b5fc-95be-49e6-988e-ca86f94927b9) — classification: Official Action Indicated (OAI), source: FDA, date: October 22, 2025
- [FDA Inspection 1067804 - Lightwave - 2018-09-26](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/140bf01d-14d8-46be-bec6-67e7f3b876b2) — classification: No Action Indicated (NAI), source: FDA, date: September 26, 2018
- [FDA Inspection 1067804 - Lightwave - 2018-09-26](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/0008c200-dd89-448b-ac1b-3feb9db73144) — classification: No Action Indicated (NAI), source: FDA, date: September 26, 2018
- [FDA Inspection 986169 - Lightwave - 2016-09-01](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/c6b1d9ee-6305-4920-b3db-d5fda4dbec82) — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2016
- [FDA Inspection 882484 - Lightwave - 2014-06-06](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/f3bc964a-373e-46b2-a86a-947547c7c1d6) — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2014
- [FDA Inspection 846387 - Lightwave - 2013-08-08](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/301c48f4-4364-4190-b0e6-bf7ae7bedb36) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 8, 2013
- [FDA Inspection 802862 - Lightwave - 2012-09-21](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/3cb8b997-e29f-47d9-b363-92bbddec2a0d) — classification: Official Action Indicated (OAI), source: FDA, date: September 21, 2012
- [FDA Inspection 802862 - Lightwave - 2012-09-21](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/0856dd97-97bf-4244-9930-4e099590b29e) — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2012
- [FDA Inspection 802862 - Lightwave - 2012-09-21](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/873f2696-99d2-43bd-9369-afccc8f7552b) — classification: Official Action Indicated (OAI), source: FDA, date: September 21, 2012

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## Related Officers

- [Scott D. Stevens](https://www.globalkeysolutions.net/people/scott-d-stevens/8d5a611a-4f0c-4e3a-9da7-3c872b08f91e)