FDA Inspection
ConMed CorportationConMed Corportation – FDA Inspection, Aug 23, 2011
Record Details
This FDA Inspection record concerns ConMed Corportation, with an inspection on August 23, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- ConMed Corportation
- Inspection Date
- August 23, 2011
- Product Type
- Devices
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ID · e4f5d472-5e48-4f10-b70f-e908af3ceb38
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 742403
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.198(c)Investigation of device failures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of ConMed Corportation
2| Date | Classification | Office | Project area |
|---|---|---|---|
| July 15, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 12, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for ConMed Corportation
- FDA Inspection 887395 - 2014-07-15
- FDA Inspection 605166 - 2009-08-12
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