FDA Warning Letter — RIGHTEYE, LLC

Case 643192 — FEI 3015176873

The FDA took a Warning Letter action against RIGHTEYE, LLC on Dec 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
Dec 20, 2022
Fiscal Year
2023
Product Type
Devices
Center
CDRH
Location
Bethesda, MD (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.