FDA issued a Warning Letter to Resonance Technology, Inc. on 4/13/2006 for a previous inspection.
483 Resonance Technology Feb 2015

483 Resonance Technology Feb 2015

Kelvin Cheung FDA$119.00 - Available Now

FDA investigators audited the Resonance Technology - Northridge, CA, United States facility and issued 3 inspectional observations (via FDA 483) on 20 Feb 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 3
  • Inspection end: 20 Feb 2015
  • Location: Northridge, United States
  • FEI: 1000306474
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