FDA Inspection 1280477 — Rayner Intraocular Lenses Limited

Rayner Intraocular Lenses Limited — FEI 3012304651

The FDA completed an inspection of Rayner Intraocular Lenses Limited on August 7, 2025 in Worthing. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 7, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Worthing (United Kingdom)

Additional Details

Sponsor, Contract Research Organization