# FDA Inspection 605166 - ConMed Corportation - August 12, 2009

Source: https://www.keypedia.com/records/fda_inspections/conmed-corportation/d27accf9-aa4e-46eb-bab7-6e10d38a5d56
Source feed: FDA_Inspections

> FDA Inspection 605166 for ConMed Corportation on August 12, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 605166
- Company Name: ConMed Corportation
- Inspection Date: 2009-08-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 887395 - 2014-07-15](https://www.keypedia.com/records/fda_inspections/conmed-corportation/43c0d9fb-4e93-4eaf-adcd-8a37e950b503)
- [FDA Inspection 742403 - 2011-08-23](https://www.keypedia.com/records/fda_inspections/conmed-corportation/e4f5d472-5e48-4f10-b70f-e908af3ceb38)

Company: https://www.keypedia.com/companies/conmed-corportation/e9801f43-5800-4aec-816e-477b6690f763

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7