FDA issued a Warning Letter to Trimed Inc on 6/30/2016 for a previous inspection.
483 TriMed Nov 2017

483 TriMed Nov 2017

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FDA investigators audited the TriMed - Santa Clarita, CA, United States facility and issued inspectional observations (via FDA 483) on 17 Nov 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 17 Nov 2017
  • Location: Santa Clarita, United States
  • FEI: 3001236812
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