FDA Inspection 1026856 - Renner & Co - September 28, 2017

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Record Details

This FDA Inspection record concerns Renner & Co, with an inspection on September 28, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Renner & Co
Inspection Date: September 28, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 026a45de-3879-4533-bc1f-2e76151dff29

Violation Codes8

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(d)21 CFR 820.2221 CFR 820.75(a)21 CFR 820.80(a)21 CFR 820.90(a)

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