# K2M, Inc. – FDA Inspection, Oct 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/k2m-inc/33219586-6ec2-4d00-90ff-26bf4d5ac100
Source feed: FDA_Inspections

> FDA inspection 1078529 of K2M, Inc., October 12, 2017. Form 483 issued. 10 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1078529
- Company Name: K2M, Inc.
- Inspection Date: 2017-10-12
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Baltimore District Office
- Citation Count: 0

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- [FDA Inspection 992904 - 2016-11-16](https://www.keypedia.com/records/fda_inspections/k2m-inc/c4c5ce42-ecd4-418c-8dc7-0f046a30700b)

Company: https://www.keypedia.com/companies/k2m-inc/03b0edf1-8ffe-422a-8877-c7bff00baa05

Office: https://www.keypedia.com/offices/baltimore-district-office/6be371ff-03e9-4039-999c-ff170f17a9fa