483 Spine Wave Jan 2017

483 Spine Wave Jan 2017

Michael Mayfield FDA$119.00 - Available Now

FDA investigators audited the Spine Wave - Shelton, CT, United States facility and issued 2 inspectional observations (via FDA 483) on 10 Jan 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 2
  • Inspection end: 10 Jan 2017
  • Location: Shelton, United States
  • FEI: 3004638600
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