FDA Inspection 786597 — Medtronic Xomed, Inc.

Medtronic Xomed, Inc. — FEI 1045254

The FDA completed an inspection of Medtronic Xomed, Inc. on Jun 6, 2012 in Jacksonville, FL. 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
Jun 6, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Jacksonville, FL (United States)