FDA Inspection 1235542 - Artegraft, Inc. - April 16, 2025

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Record Details

This FDA Inspection record concerns Artegraft, Inc., with an inspection on April 16, 2025, issued by the New Jersey District Office, covering medical devices & rad health.

Company: Artegraft, Inc.
Inspection Date: April 16, 2025
Product Type: Medical Devices & Rad Health
Office: New Jersey District Office

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ID · 5529058b-22d0-4f47-b96e-74bcbb4b63e0

Violation Codes8

21 CFR 820.100(a)21 CFR 820.18421 CFR 820.25(b)21 CFR 820.70(c)21 CFR 820.70(e)21 CFR 820.70(g)(1)21 CFR 820.75(a)21 CFR 820.75(b)

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