FDA issued a Warning Letter to Artegraft, Inc. on 5/11/2010 for a later inspection.
483 Artegraft Jun 2003

483 Artegraft Jun 2003

Frank Marciniak FDA$595.00 - Available Now

FDA investigators audited the Artegraft - North Brunswick, NJ, United States facility and issued inspectional observations (via FDA 483) on 10 Jun 2003.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 10 Jun 2003
  • Location: North Brunswick, United States
  • FEI: 1000121696
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