FDA Inspection 676161 — Synergy Health Westport, Ltd.
The FDA completed an inspection of Synergy Health Westport, Ltd. on July 20, 2010 in Westport. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 20, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Westport (Ireland)
Additional Details
Postmarket Audit Inspections