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483 Vertebral Technologies, Jun 2009

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FDA investigators audited the Vertebral Technologies - Minneapolis , MN, United States facility and issued inspectional observations (via FDA 483) on 12 Jun 2009.

Product Details

  • Category: Medical Devices & Rad Health
  • Inspection end: 12 Jun 2009
  • Location: Minneapolis, United States
  • FEI: 3007617183
Vertebral Technologies FDA inspection 483 Jun 2009

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