# FDA Inspection 992904 - K2M, Inc. - November 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/k2m-inc/99041f68-dd23-47fd-87a8-0b887c646e90
Source feed: FDA_Inspections

> FDA Inspection 992904 for K2M, Inc. on November 16, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 992904
- Company Name: K2M, Inc.
- Inspection Date: 2016-11-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: 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