FDA issued a Warning Letter to The Soule Company, Inc. on 9/15/2004 as a result of this inspection.
483 The Soule Company, dba Soule Medical Jun 2004

483 The Soule Company, dba Soule Medical Jun 2004

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FDA investigators audited the The Soule Company, dba Soule Medical - Lutz, FL, United States facility and issued inspectional observations (via FDA 483) on 18 Jun 2004.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 18 Jun 2004
  • Location: Lutz, United States
  • FEI: 1000525333
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