# FDA Inspection 808126 - M.E.E.I. Boston Keratoprosthesis - November 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/meei-boston-keratoprosthesis/23868af9-0082-4337-a044-ba8af4396a5c
Source feed: FDA_Inspections

> FDA Inspection 808126 for M.E.E.I. Boston Keratoprosthesis on November 20, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 808126
- Company Name: M.E.E.I. Boston Keratoprosthesis
- Inspection Date: 2012-11-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/meei-boston-keratoprosthesis/4c0de3d3-23da-4b9e-96f9-6c4632010fae

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