FDA issued a Warning Letter to Vertebral Technologies, Inc. on 09/04/2015 as a result of this inspection.
483 Vertebral Technologies Feb 2015
483 Vertebral Technologies Feb 2015Benjamin Anderson FDA$119.00 - Available Now
FDA investigators audited the Vertebral Technologies - Minneapolis, MN, United States facility and issued inspectional observations (via FDA 483) on 02 Feb 2015.
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- Category: Medical Devices & Rad Health
- Inspection end: 02 Feb 2015
- Location: Minneapolis, United States
- FEI: 3007617183