# FDA Inspection 706370 - K2M, Inc. - January 18, 2011

Source: https://www.keypedia.com/records/fda_inspections/k2m-inc/c8363e69-0dbd-47de-b57b-d0162b8d433c
Source feed: FDA_Inspections

> FDA Inspection 706370 for K2M, Inc. on January 18, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 706370
- Company Name: K2M, Inc.
- Inspection Date: 2011-01-18
- 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/k2m-inc/03b0edf1-8ffe-422a-8877-c7bff00baa05

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