FDA Inspection 1226943 — Medtronic MiniMed, Inc.

Medtronic MiniMed, Inc. — FEI 3003166194

The FDA completed an inspection of Medtronic MiniMed, Inc. on Jan 3, 2024 in Northridge, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 3, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Northridge, CA (United States)

Additional Details

Sponsor, Contract Research Organization

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