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

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

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Record Summary

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

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Record Information

Company

Artegraft, Inc.

Inspection Date

December 20, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f886fc8e-0ab4-4e73-9f99-13b8afb5bc39

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