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

FDA Inspection 1254940 for Herniamesh S.r.l on November 21, 2024. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1254940 for Herniamesh S.r.l on November 21, 2024. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17(a)(2)

21 CFR 820.75(a)

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Record Information

Company

Herniamesh S.r.l

Inspection Date

November 21, 2024

Product Type

Devices

Office

Center for Devices and Radiological Health

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

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