FDA Inspection 834441 — Aurora Manufacturing LLC

Aurora Manufacturing LLC — FEI 3005529226

The FDA completed an inspection of Aurora Manufacturing LLC on Apr 19, 2013 in Indianapolis, 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 19, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Indianapolis, IN (United States)