FDA issued a Warning Letter to TreyMed, Inc. on 1/9/2015 as a result of this inspection.
483 Treymed Oct 2014

483 Treymed Oct 2014

Michelle Glembin FDA, Rafael Kaup FDA$119.00 - Available Now

FDA investigators audited the Treymed - Sussex, WI, United States facility and issued 6 inspectional observations (via FDA 483) on 21 Oct 2014.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 6
  • Inspection end: 21 Oct 2014
  • Location: Sussex, United States
  • FEI: 3003007937
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