FDA Inspection 1006425 — Synergy Health North America

Synergy Health North America — FEI 1000219799

The FDA completed an inspection of Synergy Health North America on Mar 24, 2017 in Elkridge, MD. 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
Mar 24, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Elkridge, MD (United States)