FDA issued a Warning Letter to ARB Medical, LLC on 12/22/2015 as a result of this inspection.
483 ARB Medical Aug 2015

483 ARB Medical Aug 2015

Susan Matthias FDA$119.00 - Available Now

FDA investigators audited the ARB Medical - Minnetonka, MN, United States facility and issued 7 inspectional observations (via FDA 483) on 11 Aug 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 7
  • Inspection end: 11 Aug 2015
  • Location: Minnetonka, United States
  • FEI: 3005770977
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