# FDA Inspection 619791 - Linvatec Corp. dba ConMed Linvatec - October 14, 2009

Source: https://www.keypedia.com/records/fda_inspections/linvatec-corp-dba-conmed-linvatec/a11477bb-025c-4e75-8816-c1ff8d0260ab
Source feed: FDA_Inspections

> FDA Inspection 619791 for Linvatec Corp. dba ConMed Linvatec on October 14, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 619791
- Company Name: Linvatec Corp. dba ConMed Linvatec
- Inspection Date: 2009-10-14
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/linvatec-corp-dba-conmed-linvatec/1d0160a2-7161-4890-a723-4929d6219435

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