FDA Inspection 626883 - Herniamesh S.r.l - November 05, 2009

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Record Details

This FDA Inspection record concerns Herniamesh S.r.l, with an inspection on November 5, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Herniamesh S.r.l
Inspection Date: November 5, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 15f58ff6-68f6-4443-a50b-8e74aeff7420

Violation Codes4

21 CFR 803.1721 CFR 820.30(f)21 CFR 820.75(a)21 CFR 820.75(b)(2)

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