FDA Inspection 1246495 — Medtronic, Inc.

Medtronic, Inc. — FEI 3012520654

The FDA completed an inspection of Medtronic, Inc. on Aug 9, 2024 in Billerica, MA. 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
Aug 9, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Billerica, MA (United States)