FDA Inspection 553872 — Medtronic Neurosurgery

Medtronic Neurosurgery — FEI 3015531529

The FDA completed an inspection of Medtronic Neurosurgery on December 9, 2008 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
December 9, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Haltom City, TX (United States)