# FDA Inspection 613689 - M.E.E.I. Boston Keratoprosthesis - September 23, 2009

Source: https://www.keypedia.com/records/fda_inspections/meei-boston-keratoprosthesis/e5022f9a-0f4f-47db-975e-893109a8666d
Source feed: FDA_Inspections

> FDA Inspection 613689 for M.E.E.I. Boston Keratoprosthesis on September 23, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 613689
- Company Name: M.E.E.I. Boston Keratoprosthesis
- Inspection Date: 2009-09-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1024977 - 2017-07-25](https://www.keypedia.com/records/fda_inspections/meei-boston-keratoprosthesis/3b2cadb9-ed0f-4bf0-8ff9-68c72d4d03ec)
- [FDA Inspection 808126 - 2012-11-20](https://www.keypedia.com/records/fda_inspections/meei-boston-keratoprosthesis/23868af9-0082-4337-a044-ba8af4396a5c)

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