483 Turbo Wheelchair May 2017

483 Turbo Wheelchair May 2017

Shannon Gregory FDA$119.00 - Available Now

FDA investigators audited the Turbo Wheelchair - Louisville, KY, United States facility and issued inspectional observations (via FDA 483) on 02 May 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 02 May 2017
  • Location: Louisville, United States
  • FEI: 3004149089
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