FDA Inspection 1254940 - Herniamesh S.r.l - November 21, 2024

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Record Details

This FDA Inspection record concerns Herniamesh S.r.l, with an inspection on November 21, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company: Herniamesh S.r.l
Inspection Date: November 21, 2024
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · f8420bab-0187-4b06-bb1e-40aee1b4936e

Violation Codes2

21 CFR 803.17(a)(2)21 CFR 820.75(a)

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