FDA Inspection 595880 — Medtronic Inc

Medtronic Inc — FEI 3004185781

The FDA completed an inspection of Medtronic Inc on Jul 10, 2009 in Tempe, AZ. 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
Jul 10, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Tempe, AZ (United States)