FDA Inspection 802887 - Klockner Of North America - October 03, 2012

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Record Details

This FDA Inspection record concerns Klockner Of North America, with an inspection on October 3, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Klockner Of North America
Inspection Date: October 3, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 3aba4384-e2a2-46cf-8dbc-44a76c4aaa14

Violation Codes1

21 CFR 820.198(a)

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