FDA Inspection 996804 — Alevio, LLC

Alevio, LLC — FEI 3012249461

The FDA completed an inspection of Alevio, LLC on December 15, 2016 in Cullman, AL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 15, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Cullman, AL (United States)