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