FDA issued a Warning Letter to Electro Medical, Inc on 8/9/2013 as a result of this inspection.
483 Electro Medical Apr 2013

483 Electro Medical Apr 2013

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FDA investigators audited the Electro Medical - Tulsa, OK, United States facility and issued inspectional observations (via FDA 483) on 19 Apr 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 19 Apr 2013
  • Location: Tulsa, United States
  • FEI: 1000117937
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