FDA Inspection 1044249 — Medtronic MiniMed, Inc.
The FDA completed an inspection of Medtronic MiniMed, Inc. on Mar 14, 2018 in Northridge, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Mar 14, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Northridge, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3172 | 21 CFR 820.198(c) | Investigation of device failures |
| 732 | 21 CFR 803.50(a)(2) | Individual Report of Malfunction |