FDA issued a Warning Letter to Sybaritic, Incorporated on 9/1/2004 for a previous inspection.
483 Sybaritic Mar 2009

483 Sybaritic Mar 2009

Aaron Dunbar FDA, Heather Kleimola Hulbert FDA$119.00 - Available Now

FDA investigators audited the Sybaritic - Bloomington, MN, United States facility and issued inspectional observations (via FDA 483) on 30 Mar 2009.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 30 Mar 2009
  • Location: Bloomington, United States
  • FEI: 2131125
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