FDA issued a Warning Letter to Diomedics, Inc. on 3/29/2004 for a previous inspection.
483 Diomedics Nov 2012

483 Diomedics Nov 2012

Randall Morris FDA, Richard Vogel FDA$119.00 - Available Now

FDA investigators audited the Diomedics - Waldo, FL, United States facility and issued 2 inspectional observations (via FDA 483) on 06 Nov 2012.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 2
  • Inspection end: 06 Nov 2012
  • Location: Waldo, United States
  • FEI: 1000222160
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