483 SURESTEP Aug 2015

483 SURESTEP Aug 2015

Cynthia Li FDA, Cynthia Aycock FDA$119.00 - Available Now

FDA investigators audited the SURESTEP - South Bend, IN, United States facility and issued inspectional observations (via FDA 483) on 05 Aug 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 05 Aug 2015
  • Location: South Bend, United States
  • FEI: 3003895329
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