FDA Inspection 1023356 - KCI USA, Inc. - April 21, 2017

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Record Details

This FDA Inspection record concerns KCI USA, Inc., with an inspection on April 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: KCI USA, Inc.
Inspection Date: April 21, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0b9b9074-0a82-4e36-aa55-29f3d8fa41cf