FDA issued a Warning Letter to Resonance Technology, Inc. on 4/13/2006 as a result of this inspection.
483 Resonance Technology Jan 2006

483 Resonance Technology Jan 2006

Leonard Lavi FDA$119.00 - Available Now

FDA investigators audited the Resonance Technology - Northridge, CA, United States facility and issued inspectional observations (via FDA 483) on 27 Jan 2006.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 27 Jan 2006
  • Location: Northridge, United States
  • FEI: 1000306474
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