FDA Inspection
ConMed CorporationConMed Corporation – FDA Inspection, Jul 18, 2014
Record Details
This FDA Inspection record concerns ConMed Corporation, with an inspection on July 18, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- ConMed Corporation
- Inspection Date
- July 18, 2014
- Product Type
- Devices
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ID · 401b2786-024a-4744-b8b9-9e766f776def
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 890625
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.72(a)Equipment control activity documentation
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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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 |
| April 26, 2012 | 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 781540 - 2012-04-26
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