FDA issued a Warning Letter to US Vascular LLC on 6/7/2018 for a previous inspection.
483 US Vascular Feb 2020

483 US Vascular Feb 2020

Paul Kawamoto FDA$119.00 - Available Now

FDA investigators audited the US Vascular - Beaverton, OR, United States facility and issued inspectional observations (via FDA 483) on 13 Feb 2020.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 13 Feb 2020
  • Location: Beaverton, United States
  • FEI: 3010089756
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