FDA Inspection
Medtronic Vascular, Inc.Medtronic Vascular, Inc. – FDA Inspection, Oct 30, 2008
Record Details
This FDA Inspection record concerns Medtronic Vascular, Inc., with an inspection on October 30, 2008, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medtronic Vascular, Inc.
- Inspection Date
- October 30, 2008
- Product Type
- Devices
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ID · ade6a742-6e11-4f68-8688-115c4d01cefb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 546657
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.40(b)Changes, communication
- 21 CFR 820.90(b)(1)Documentation of disposition, justification, signature
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Other FDA inspections of Medtronic Vascular, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 15, 2021 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 2, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 27, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 24, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medtronic Vascular, Inc.
- FDA Inspection 1155023 - 2021-10-15
- FDA Inspection 973289 - 2016-06-02
- FDA Inspection 829995 - 2013-02-27
- FDA Inspection 710946 - 2011-02-24
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