FDA issued a Warning Letter to Ventlab LLC on 7/2/2014 as a result of this inspection.
FDA investigators audited the Ventlab - Grand Rapids, MI, United States facility and issued inspectional observations (via FDA 483) on 04 Jun 2014.
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- Category: Medical Devices & Rad Health
- Inspection end: 04 Jun 2014
- Location: Grand Rapids, United States
- FEI: 2246980