FDA Inspection
AtriCure, Inc.AtriCure, Inc. – FDA Inspection, Feb 22, 2011
Record Details
This FDA Inspection record concerns AtriCure, Inc., with an inspection on February 22, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- AtriCure, Inc.
- Inspection Date
- February 22, 2011
- Product Type
- Devices
View Company Profile
ID · a42eadda-ec38-4647-8c93-0a7337536200
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 713759
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
Other FDA inspections of AtriCure, Inc.
11| Date | Classification | Office | Project area |
|---|---|---|---|
| December 13, 2018 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 9, 2018 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 9, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 5, 2017 | Not classified | Cincinnati District Office | |
| August 24, 2017 | Not classified | Cincinnati District Office |
Other documents for AtriCure, Inc.
- FDA Inspection 1077020 - 2018-12-13
- FDA Inspection 1055553 - 2018-03-09
- FDA Inspection 1043957 - 2018-03-09
- FDA Inspection 1042648 - 2017-10-05
- FDA Inspection 1045711 - 2017-08-24
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