FDA Inspection 811367 — Medtronic Neurosurgery

Medtronic Neurosurgery — FEI 3015531529

The FDA completed an inspection of Medtronic Neurosurgery on November 21, 2012 in Haltom City, TX. 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
November 21, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Haltom City, TX (United States)