# RIGHTEYE, LLC – FDA Inspection, Mar 8, 2024

Source: https://www.keypedia.com/records/fda_inspections/righteye-llc/5ea0003c-3bcc-4be4-9673-10f0a4ae251d
Source feed: FDA_Inspections

> FDA inspection 1232251 of RIGHTEYE, LLC, March 08, 2024. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1232251
- Company Name: RIGHTEYE, LLC
- Inspection Date: 2024-03-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1173902 - 2022-07-08](https://www.keypedia.com/records/fda_inspections/righteye-llc/2e85c482-23ea-40a0-b3d8-7b4092b8f7a4)

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

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