FDA issued a Warning Letter to Xoran Technologies Inc on 3/25/2008 for a previous inspection.
483 Xoran Technologies May 2012

483 Xoran Technologies May 2012

Thomas Peter FDA, Sargum Sood FDA$119.00 - Available Now

FDA investigators audited the Xoran Technologies - Ann Arbor, MI, United States facility and issued inspectional observations (via FDA 483) on 14 May 2012.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 14 May 2012
  • Location: Ann Arbor, United States
  • FEI: 3004198450
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