FDA Inspection 1024977 - M.E.E.I. Boston Keratoprosthesis - July 25, 2017

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Record Details

This FDA Inspection record concerns M.E.E.I. Boston Keratoprosthesis, with an inspection on July 25, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: M.E.E.I. Boston Keratoprosthesis
Inspection Date: July 25, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 3b2cadb9-ed0f-4bf0-8ff9-68c72d4d03ec

FDA Inspection

M.E.E.I. Boston KeratoprosthesisJuly 25, 2017