FDA issued a Warning Letter to Maquet Cardiovascular, LLC on 8/11/2010 for a later inspection.
483 Maquet Cardiovascular Apr 2009

483 Maquet Cardiovascular Apr 2009

Robert Ruff FDA$119.00 - Available Now

FDA investigators audited the Maquet Cardiovascular - Wayne, NJ, United States facility and issued inspectional observations (via FDA 483) on 17 Apr 2009.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 17 Apr 2009
  • Location: Wayne, United States
  • FEI: 2242352
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