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

Source: https://www.globalkeysolutions.net/records/fda_inspections/artegraft-inc/fc0624e3-73df-4afa-99ca-5e58fe389339/
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1202728
- Company Name: Artegraft, Inc.
- Inspection Date: 2023-04-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/artegraft-inc/ea31640f-5897-4972-8d68-16ea7ca1d8eb

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7