# FDA Inspection 704445 - Artegraft, Inc. - December 20, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/artegraft-inc/f886fc8e-0ab4-4e73-9f99-13b8afb5bc39/
Source feed: FDA_Inspections

> FDA Inspection 704445 for Artegraft, Inc. on December 20, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 704445
- Company Name: Artegraft, Inc.
- Inspection Date: 2010-12-20
- 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.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