FDA Inspection 821337 - Protech Professional Products, Inc. - February 27, 2013

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Record Details

This FDA Inspection record concerns Protech Professional Products, Inc., with an inspection on February 27, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Protech Professional Products, Inc.
Inspection Date: February 27, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 091ca62f-97d8-4367-acd7-75b779af682c

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.12021 CFR 820.18421 CFR 820.198(a)21 CFR 820.25(a)21 CFR 820.30(a)21 CFR 820.4021 CFR 820.5021 CFR 820.70(a)

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