FDA Inspection 937481 - Herniamesh S.r.l - July 23, 2015

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Record Details

This FDA Inspection record concerns Herniamesh S.r.l, with an inspection on July 23, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Herniamesh S.r.l
Inspection Date: July 23, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 05393c35-1e31-4beb-bde9-75f13ebb51ad

Violation Codes8

21 CFR 803.50(a)(2)21 CFR 820.15021 CFR 820.198(a)21 CFR 820.2221 CFR 820.250(b)21 CFR 820.70(i)21 CFR 820.72(b)21 CFR 820.75(a)

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