FDA issued a Warning Letter to Vevazz LLC on 12/26/2019 as a result of this inspection.
FDA investigators audited the Vevazz - Eaton, CO, United States facility and issued inspectional observations (via FDA 483) on 20 Jun 2019.
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- Category: Medical Devices & Rad Health
- Inspection end: 20 Jun 2019
- Location: Eaton, United States
- FEI: 3009690171