# FDA Inspection 816080 - Artegraft, Inc. - January 25, 2013

Source: https://www.keypedia.com/records/fda_inspections/artegraft-inc/55e30f43-2271-4916-ae98-92d1e95a9df0
Source feed: FDA_Inspections

> FDA Inspection 816080 for Artegraft, Inc. on January 25, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 816080
- Company Name: Artegraft, Inc.
- Inspection Date: 2013-01-25
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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