# FDA Inspection 1291402 - Lightwave - October 22, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/lightwave/2996b5fc-95be-49e6-988e-ca86f94927b9
Source feed: FDA_Inspections

> FDA Inspection 1291402 for Lightwave on October 22, 2025. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1291402
- Company Name: Lightwave
- Inspection Date: 2025-10-22
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Denver District Office

## Related Documents

- [FDA Inspection 1291402 - 2025-10-22](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/cbc2c446-e7cd-4410-9cb5-fe0399908836)
- [FDA Inspection 1067804 - 2018-09-26](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/140bf01d-14d8-46be-bec6-67e7f3b876b2)
- [FDA Inspection 1067804 - 2018-09-26](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/0008c200-dd89-448b-ac1b-3feb9db73144)
- [FDA Inspection 986169 - 2016-09-01](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/c6b1d9ee-6305-4920-b3db-d5fda4dbec82)
- [FDA Inspection 882484 - 2014-06-06](https://www.globalkeysolutions.net/records/fda_inspections/lightwave/f3bc964a-373e-46b2-a86a-947547c7c1d6)

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

Office: https://www.globalkeysolutions.net/offices/denver-district-office/93b79063-390c-4759-af6c-5da7e388face