FDA Inspection
Vertos Medical, Inc.Vertos Medical, Inc. – FDA Inspection, May 26, 2009
Record Details
This FDA Inspection record concerns Vertos Medical, Inc., with an inspection on May 26, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Vertos Medical, Inc.
- Inspection Date
- May 26, 2009
- Product Type
- Devices
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ID · 79e0ee41-88c6-47a2-86e0-ac8d58299bfb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 586318
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(a)(3)Identification of actions needed
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
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Other FDA inspections of Vertos Medical, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| April 5, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 17, 2020 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 10, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 25, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Vertos Medical, Inc.
- FDA Inspection 1205079 - 2023-04-05
- FDA Inspection 1122345 - 2020-03-17
- FDA Inspection 992059 - 2016-11-10
- FDA Inspection 842491 - 2013-07-25
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