FDA Inspection 1089775 — Synergy Health Ede BV

Synergy Health Ede BV — FEI 3002807038

The FDA completed an inspection of Synergy Health Ede BV on Feb 7, 2019 in Ede. 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
Feb 7, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Ede (Netherlands)

Additional details

Postmarket Audit Inspections

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.