FDA issued a Warning Letter to Westone Laboratories Incorporated on 10/23/2012 for a previous inspection.
483 Westone Labs Nov 2017

483 Westone Labs Nov 2017

Vicky Cruz FDA$119.00 - Available Now

FDA investigators audited the Westone Labs - Colorado Springs, CO, United States facility and issued inspectional observations (via FDA 483) on 15 Nov 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 15 Nov 2017
  • Location: Colorado Springs, United States
  • FEI: 2094377
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