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FDA Inspection 907242 — Medtronic MiniMed, Inc.

Medtronic MiniMed, Inc. — FEI 3003166194

The FDA completed an inspection of Medtronic MiniMed, Inc. on November 21, 2014 in Northridge, CA. 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, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Northridge, CA (United States)

Additional Details

Postmarket Audit Inspections

Facility

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Recent compliance actions

FDA data resources