FDA Inspection 907242 — Medtronic MiniMed, Inc.
The FDA completed an inspection of Medtronic MiniMed, Inc. on Nov 21, 2014 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
- Nov 21, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Northridge, CA (United States)
Additional Details
Postmarket Audit Inspections