FDA Inspection 843139 - Vioptix, Inc. - August 05, 2013

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Record Details

This FDA Inspection record concerns Vioptix, Inc., with an inspection on August 5, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vioptix, Inc.
Inspection Date: August 5, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 72e4f250-27cf-42e1-85c9-38e626410b1d