# K2M, Inc. – FDA Inspection, Nov 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/k2m-inc/c4c5ce42-ecd4-418c-8dc7-0f046a30700b
Source feed: FDA_Inspections

> FDA inspection 992904 of K2M, Inc., November 16, 2016. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 10 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 992904
- Company Name: K2M, Inc.
- Inspection Date: 2016-11-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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## Related Officers

- [Investigator](https://www.keypedia.com/people/shannon-a-gregory/3e791321-dced-4e1d-89a1-3da91d577961)

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