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FDA Inspection 1082648 — Medtronic MiniMed, Inc.

Medtronic MiniMed, Inc. — FEI 3003166194

The FDA completed an inspection of Medtronic MiniMed, Inc. on February 15, 2019 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
February 15, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Northridge, CA (United States)

Facility

Other inspections at this facility

  • 1226943 (NAI Wed Jan 03 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1199488 (NAI Fri Mar 10 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1145642 (OAI Wed Jul 07 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1044249 (VAI Wed Mar 14 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022946 (NAI Mon Aug 14 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources