FDA Inspection 952967 — Synergy Health Ede BV

Synergy Health Ede BV — FEI 3002807038

The FDA completed an inspection of Synergy Health Ede BV on Dec 3, 2015 in Ede. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection details

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

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