FDA Inspection 1202728 - Artegraft, Inc. - April 13, 2023

FDA Inspection 1202728 for Artegraft, Inc. on April 13, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1202728 for Artegraft, Inc. on April 13, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Artegraft, Inc.

Inspection Date

April 13, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc0624e3-73df-4afa-99ca-5e58fe389339

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