FDA Inspection 1008842 - Percussionaire Corporation - March 24, 2017

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Record Details

This FDA Inspection record concerns Percussionaire Corporation, with an inspection on March 24, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Percussionaire Corporation
Inspection Date: March 24, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b5ae33c8-597a-4584-9c17-ffc23ae5fff2

Violation Codes4

21 CFR 803.50(a)(2)21 CFR 820.100(a)21 CFR 820.4021 CFR 820.72(b)

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