FDA Inspection
ConMed CorporationConMed Corporation – FDA Inspection, Apr 26, 2012
Record Details
This FDA Inspection record concerns ConMed Corporation, with an inspection on April 26, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- ConMed Corporation
- Inspection Date
- April 26, 2012
- Product Type
- Devices
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ID · 861f80b3-7660-498f-8c5d-734348271abb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 781540
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Complaints
- 21 CFR 820.100(b)Documentation
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Other FDA inspections of ConMed Corporation
7| Date | Classification | Office | Project area |
|---|---|---|---|
| July 13, 2022 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 22, 2020 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 3, 2017 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 3, 2016 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 18, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for ConMed Corporation
- FDA Inspection 1175139 - 2022-07-13
- FDA Inspection 1129759 - 2020-09-22
- FDA Inspection 999612 - 2017-02-03
- FDA Inspection 963326 - 2016-02-03
- FDA Inspection 890625 - 2014-07-18
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