FDA Inspection 1066892 - Kennametal Stellite L.P. - September 26, 2018

Record Details

This FDA Inspection record concerns Kennametal Stellite L.P., with an inspection on September 26, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kennametal Stellite L.P.
Inspection Date: September 26, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6c73cdfa-251d-47b7-8b50-f7a7241c4233

Violation Codes1

21 CFR 820.184

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