FDA Inspection 571879 — Alivio Corporation

Alivio Corporation — FEI 3004976979

The FDA completed an inspection of Alivio Corporation on February 26, 2009 in Ada, MI. 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
February 26, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Ada, MI (United States)