# FDA Inspection 1173902 - RIGHTEYE, LLC - July 08, 2022

Source: https://www.keypedia.com/records/fda_inspections/righteye-llc/787acad2-b6c3-4759-9f34-48e78439bf64
Source feed: FDA_Inspections

> FDA Inspection 1173902 for RIGHTEYE, LLC on July 08, 2022. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1173902
- Company Name: RIGHTEYE, LLC
- Inspection Date: 2022-07-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1232251 - 2024-03-08](https://www.keypedia.com/records/fda_inspections/righteye-llc/5ea0003c-3bcc-4be4-9673-10f0a4ae251d)
- [FDA Inspection 1232251 - 2024-03-08](https://www.keypedia.com/records/fda_inspections/righteye-llc/46cff2a7-1215-459a-8e4e-8f572981a440)
- [FDA Inspection 1173902 - 2022-07-08](https://www.keypedia.com/records/fda_inspections/righteye-llc/2e85c482-23ea-40a0-b3d8-7b4092b8f7a4)

Company: https://www.keypedia.com/companies/righteye-llc/bca3f1bc-4f9c-44b8-8436-ac9a14dbb5f2

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7