FDA Inspection 580993 — Avalign Delivery Systems Division

Avalign Delivery Systems Division — FEI 3000717687

The FDA completed an inspection of Avalign Delivery Systems Division on Apr 30, 2009 in Greenwood, IN. 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
Apr 30, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Greenwood, IN (United States)