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FDA Inspection 821664 — Medtronic MiniMed, Inc.

Medtronic MiniMed, Inc. — FEI 3003166194

The FDA completed an inspection of Medtronic MiniMed, Inc. on April 12, 2013 in Northridge, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
April 12, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Northridge, CA (United States)

Facility

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Recent compliance actions

FDA data resources