FDA Inspection 819271 — Synergy Health North America

Synergy Health North America — FEI 1000219799

The FDA completed an inspection of Synergy Health North America on Feb 21, 2013 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
Feb 21, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Elkridge, MD (United States)