FDA Inspection 584459 — GyNova, LLC
The FDA completed an inspection of GyNova, LLC on May 26, 2009 in Manchester, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- May 26, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Manchester, CT (United States)