FDA Inspection
Rayner Intraocular Lenses LtdRayner Intraocular Lenses Ltd – FDA Inspection, Apr 26, 2018
Record Details
This FDA Inspection record concerns Rayner Intraocular Lenses Ltd, with an inspection on April 26, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c390112b-49dc-432e-9d1b-9ba98781fd10
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1050301
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
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Other FDA inspections of Rayner Intraocular Lenses Ltd
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 7, 2025 | Not classified | Office of Inspections and Investigations |
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