FDA Inspection 1089775 — Synergy Health Ede BV
The FDA completed an inspection of Synergy Health Ede BV on February 7, 2019 in Ede. 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
- February 7, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Ede (Netherlands)
Additional Details
Postmarket Audit Inspections