FDA Inspection 952967 — Synergy Health Ede BV

Synergy Health Ede BV — FEI 3002807038

The FDA completed an inspection of Synergy Health Ede BV on December 3, 2015 in Ede. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 3, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Ede (Netherlands)