FDA issued a Warning Letter to Artegraft, Inc. on 5/11/2010 for a previous inspection.
483 Artegraft Jan 2015

483 Artegraft Jan 2015

Frank Marciniak FDA$119.00 - Available Now

FDA investigators audited the Artegraft - North Brunswick, NJ, United States facility and issued 4 inspectional observations (via FDA 483) on 28 Jan 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 4
  • Inspection end: 28 Jan 2015
  • Location: North Brunswick, United States
  • FEI: 1000121696
Add To Cart