FDA Warning Letter — RIGHTEYE, LLC

Case 643192 — FEI 3015176873

The FDA took a Warning Letter action against RIGHTEYE, LLC on December 20, 2022 (Bethesda, MD). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
RIGHTEYE, LLC
Date
December 20, 2022
Fiscal Year
2023
Product Type
Devices
Center
CDRH
Location
Bethesda, MD (United States)