FDA issued a Warning Letter to Artegraft, Inc. on 5/11/2010 for a previous inspection.
483 Artegraft Dec 2010

483 Artegraft Dec 2010

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

Product details

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