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FDA Inspection 952080 — Synergy Health Ede BV

Synergy Health Ede BV — FEI 3009337401

The FDA completed an inspection of Synergy Health Ede BV on Nov 13, 2015 in Venlo. 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
Nov 13, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Venlo (Netherlands)

Facility

FDA data resources

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