FDA Inspection 1071279 - Fibralign Corporation - November 08, 2018

Record Details

This FDA Inspection record concerns Fibralign Corporation, with an inspection on November 8, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Fibralign Corporation
Inspection Date: November 8, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 68a5897d-1f1a-4159-91e2-99db0e813987