FDA Inspection 1199488 — Medtronic MiniMed, Inc.

Medtronic MiniMed, Inc. — FEI 3003166194

The FDA completed an inspection of Medtronic MiniMed, Inc. on March 10, 2023 in Northridge, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 10, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Northridge, CA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures