FDA Inspection 996935 - Karl Storz Endovision, Inc. - December 20, 2016

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Record Details

This FDA Inspection record concerns Karl Storz Endovision, Inc., with an inspection on December 20, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Karl Storz Endovision, Inc.
Inspection Date: December 20, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 3376edf3-97d0-4e82-bc38-ff25eef8e545

Violation Codes1

21 CFR 820.86

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