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483 Maquet Cardiovascular, Apr 2009

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by Robert Ruff FDA

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

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Product Details

  • Inspection end: 17 Apr 2009
  • Location: Wayne, United States
  • FEI: 2242352
Maquet Cardiovascular FDA inspection 483 Apr 2009

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