FDA issued a Warning Letter to Anulex Technologies, Inc. on 2/11/2011 as a result of this inspection.
483 Anulex Technologies Sep 2010

483 Anulex Technologies Sep 2010

$119 - Not in Stock

FDA investigators audited the Anulex Technologies - Eden Prairie, MN, United States facility and issued inspectional observations (via FDA 483) on 22 Sep 2010.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 22 Sep 2010
  • Location: Eden Prairie, United States
  • FEI: 3005501497
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