FDA Inspection
Medtronic Inc.Medtronic Inc. – FDA Inspection, Sep 2, 2010
Record Details
This FDA Inspection record concerns Medtronic Inc., with an inspection on September 2, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medtronic Inc.
- Inspection Date
- September 2, 2010
- Product Type
- Devices
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ID · b182845a-17b1-45a4-baf3-9c2eae96625d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 679423
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of Medtronic Inc.
16| Date | Classification | Office | Project area |
|---|---|---|---|
| February 10, 2025 | VAI | Minneapolis District Office | Compliance: Medical Devices |
| September 1, 2023 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| February 4, 2020 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| August 16, 2018 | Not classified | Minneapolis District Office | |
| May 14, 2018 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medtronic Inc.
- FDA Inspection 1250873 - 2025-02-10
- FDA Inspection 1217414 - 2023-09-01
- FDA Inspection 1118989 - 2020-02-04
- FDA Inspection 1157919 - 2018-08-16
- FDA Inspection 1052017 - 2018-05-14
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