FDA Inspection 766195 — Medtronic Spine & Biologics

Medtronic Spine & Biologics — FEI 3006717083

The FDA completed an inspection of Medtronic Spine & Biologics on Dec 20, 2011 in Oak Brook, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 20, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Oak Brook, IL (United States)