# FDA Inspection 1269039 - Luminopia Inc - May 02, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/luminopia-inc/e9840992-660b-4af7-94cd-08879625e777
Source feed: FDA_Inspections

> FDA Inspection 1269039 for Luminopia Inc on May 02, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1269039
- Company Name: Luminopia Inc
- Inspection Date: 2025-05-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New England District Office

## Related Documents

- [FDA Inspection 1269039 - 2025-05-02](https://www.globalkeysolutions.net/records/fda_inspections/luminopia-inc/6b5f39e0-c06f-4362-8d74-1203ec902495)
- [FDA Inspection 1269039 - 2025-05-02](https://www.globalkeysolutions.net/records/fda_inspections/luminopia-inc/1f26da1f-4e23-41b5-a040-63360bbf296e)
- [FDA Inspection 1269039 - 2025-05-02](https://www.globalkeysolutions.net/records/fda_inspections/luminopia-inc/bccf6236-0235-4052-b902-e87d94afd4ec)

Company: https://www.globalkeysolutions.net/companies/luminopia-inc/87a7149c-d5ef-4106-824e-f28304e12e12

Office: https://www.globalkeysolutions.net/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144