483 DT MedTech Oct 2017

483 DT MedTech Oct 2017

James Simpson FDA, Katelyn Staub-Zamperini FDA, Daniel Tammariello FDA$119.00 - Available Now

FDA investigators audited the DT MedTech - Towson, MD, United States facility and issued inspectional observations (via FDA 483) on 24 Oct 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 24 Oct 2017
  • Location: Towson, United States
  • FEI: 3012104767
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