FDA issued a Warning Letter to Isolux, LLC on 1/8/2016 for a later inspection.
483 Isolux Jan 2010

483 Isolux Jan 2010

Nicole Knowlton FDA, Joshua Silvestri FDA$119.00 - Available Now

FDA investigators audited the Isolux - Naples, FL, United States facility and issued inspectional observations (via FDA 483) on 22 Jan 2010.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 22 Jan 2010
  • Location: Naples, United States
  • FEI: 3002249830
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