FDA issued a Warning Letter to ARB Medical, LLC on 12/22/2015 as a result of this inspection.
FDA investigators audited the ARB Medical - Minnetonka, MN, United States facility and issued 7 inspectional observations (via FDA 483) on 11 Aug 2015.
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- Category: Medical Devices & Rad Health
- Number of Observations: 7
- Inspection end: 11 Aug 2015
- Location: Minnetonka, United States
- FEI: 3005770977