FDA issued a Warning Letter to GyNova LLC on 1/31/2008 as a result of this inspection.
FDA investigators audited the GyNova - Manchester, CT, United States facility and issued inspectional observations (via FDA 483) on 05 Nov 2007.
Add To Cart
- Category: Medical Devices & Rad Health
- Inspection end: 05 Nov 2007
- Location: Manchester, United States
- FEI: 3005718321