FDA Inspection 1080319 - STERITECH, INC. - February 19, 2019

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Record Details

This FDA Inspection record concerns STERITECH, INC., with an inspection on February 19, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: STERITECH, INC.
Inspection Date: February 19, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 65659195-bad0-4589-9040-e2503212f011

Violation Codes5

21 CFR 820.100(a)21 CFR 820.100(b)21 CFR 820.4021 CFR 820.70(a)21 CFR 820.72(a)

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