FDA Inspection 1325342 - Artegraft, Inc. - June 25, 2026

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Record Details

This FDA Inspection record concerns Artegraft, Inc., with an inspection on June 25, 2026, issued by the New Jersey District Office, covering medical devices & rad health.

Company: Artegraft, Inc.
Inspection Date: June 25, 2026
Product Type: Medical Devices & Rad Health
Office: New Jersey District Office

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ID · 042f5669-93b7-4704-a81e-2afc48e7f814

Violation Codes8

ISO 13485:2016 Clause 6.4.2ISO 13485:2016 Clause 7.3.3ISO 13485:2016 Clause 7.5.1ISO 13485:2016 Clause 7.5.11ISO 13485:2016 Clause 8.2.1ISO 13485:2016 Clause 8.3.1ISO 13485:2016 Clause 8.5.2ISO 13485:2016 Clause 8.5.3

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