# Artegraft, Inc. – FDA Inspection, Jan 28, 2015

Source: https://www.keypedia.com/records/fda_inspections/artegraft-inc/acb41225-09ea-4d50-b723-0472b004f196
Source feed: FDA_Inspections

> FDA inspection 911848 of Artegraft, Inc., January 28, 2015. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 911848
- Company Name: Artegraft, Inc.
- Inspection Date: 2015-01-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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

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