FDA Inspection 1030896 — EGlobal, LLC

EGlobal, LLC — FEI 3013501546

The FDA completed an inspection of EGlobal, LLC on Oct 13, 2017 in Scottsdale, AZ. 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
Oct 13, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Scottsdale, AZ (United States)