# FDA Inspection 1224877 - Midwest Eye Laboratories Inc - December 13, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/midwest-eye-laboratories-inc/ce872125-f969-402b-b73e-d90e513234ae
Source feed: FDA_Inspections

> FDA Inspection 1224877 for Midwest Eye Laboratories Inc on December 13, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1224877
- Company Name: Midwest Eye Laboratories Inc
- Inspection Date: 2023-12-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1224877 - 2023-12-13](https://www.globalkeysolutions.net/records/fda_inspections/midwest-eye-laboratories-inc/6f09021b-76fb-442f-b620-a7526908f8eb)
- [FDA Inspection 582250 - 2009-05-11](https://www.globalkeysolutions.net/records/fda_inspections/midwest-eye-laboratories-inc/a45c1c98-be46-4cfc-9b19-7bcf962bf0d8)

Company: https://www.globalkeysolutions.net/companies/midwest-eye-laboratories-inc/9348bce9-ea37-4aea-9793-bdf3e26caf44

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