FDA issued a Warning Letter to GyNova LLC on 1/31/2008 as a result of this inspection.
483 GyNova Nov 2007

483 GyNova Nov 2007

Edward Janik FDA$119.00 - Available Now

FDA investigators audited the GyNova - Manchester, CT, United States facility and issued inspectional observations (via FDA 483) on 05 Nov 2007.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 05 Nov 2007
  • Location: Manchester, United States
  • FEI: 3005718321
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