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