FDA Inspection 1050301 — Rayner Intraocular Lenses Limited
The FDA completed an inspection of Rayner Intraocular Lenses Limited on April 26, 2018 in Worthing. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- April 26, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Worthing (United Kingdom)