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483 Artegraft, Dec 2010

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by Kinh Mac FDA

FDA investigators audited the Artegraft - North Brunswick , NJ, United States facility and issued inspectional observations (via FDA 483) on 20 Dec 2010.

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Product Details

  • Category: Medical Devices & Rad Health
  • Inspection end: 20 Dec 2010
  • Location: North Brunswick, United States
  • FEI: 1000121696
Artegraft FDA inspection 483 Dec 2010

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