FDA Inspection
Medtronic MiniMed, Inc.Medtronic MiniMed, Inc. – FDA Inspection, Dec 16, 2013
Record Details
This FDA Inspection record concerns Medtronic MiniMed, Inc., with an inspection on December 16, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medtronic MiniMed, Inc.
- Inspection Date
- December 16, 2013
- Product Type
- Devices
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ID · ebc60511-8c0d-4598-9352-8a079ce064d6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 859043
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.140(b)(5)Sponsor records of adverse device effects & complaints
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Medtronic MiniMed, Inc.
13| Date | Classification | Office | Project area |
|---|---|---|---|
| January 3, 2024 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 10, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 7, 2021 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 15, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 14, 2018 | VAI | Center for Devices and Radiological Health | Project Evaluation: Devices |
Other documents for Medtronic MiniMed, Inc.
- FDA Inspection 1226943 - 2024-01-03
- FDA Inspection 1199488 - 2023-03-10
- FDA Inspection 1145642 - 2021-07-07
- FDA Inspection 1082648 - 2019-02-15
- FDA Inspection 1044249 - 2018-03-14
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