# FDA Inspection 1050301 - Rayner Intraocular Lenses Ltd - April 26, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/rayner-intraocular-lenses-ltd/391821d6-6018-4aa9-8112-253acfdbf92c
Source feed: FDA_Inspections

> FDA Inspection 1050301 for Rayner Intraocular Lenses Ltd on April 26, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050301
- Company Name: Rayner Intraocular Lenses Ltd
- Inspection Date: 2018-04-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1050301 - 2018-04-26](https://www.globalkeysolutions.net/records/fda_inspections/rayner-intraocular-lenses-ltd/c390112b-49dc-432e-9d1b-9ba98781fd10)

Company: https://www.globalkeysolutions.net/companies/rayner-intraocular-lenses-ltd/54db1d10-6224-4528-84cd-2e8f28d3532c

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7