FDA issued a Warning Letter to Ferno-Washington, Inc on 4/7/2006 as a result of this inspection.
483 Ferno-Washington Sep 2005

483 Ferno-Washington Sep 2005

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FDA investigators audited the Ferno-Washington - Wilmington, OH, United States facility and issued inspectional observations (via FDA 483) on 30 Sep 2005.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 30 Sep 2005
  • Location: Wilmington, United States
  • FEI: 1523574
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