# K2M, Inc. - Inspection Records

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

> Inspection records and compliance data for K2M, Inc. in Leesburg, Virginia. Access full analysis and detailed observations.

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## Details

- Name: K2M, Inc.
- FEI Number: 3008599177
- City: Leesburg
- State: Virginia
- Country Name: United States
- Address Line 1: 600 Hope Pkwy Se
- Zip Code: 20175

## Related Documents

- [FDA Inspection 1236122 - K2M, Inc. - 2024-03-21](https://www.keypedia.com/records/fda_inspections/k2m-inc/1491f2aa-dc22-4c8a-8da9-9416a1017c6a) — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2024
- [FDA Inspection 1236122 - K2M, Inc. - 2024-03-21](https://www.keypedia.com/records/fda_inspections/k2m-inc/f68d2bb0-b6ae-427f-bad7-c45a44794b12) — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2024
- [FDA Inspection 1168720 - K2M, Inc. - 2022-04-21](https://www.keypedia.com/records/fda_inspections/k2m-inc/f906299b-b489-43e7-b08f-c5e5a1ecb771) — classification: No Action Indicated (NAI), source: FDA, date: April 21, 2022
- [FDA Inspection 1168720 - K2M, Inc. - 2022-04-21](https://www.keypedia.com/records/fda_inspections/k2m-inc/20052a4b-17f4-4a55-a964-c1a53562e75d) — classification: No Action Indicated (NAI), source: FDA, date: April 21, 2022
- [FDA Inspection 1148726 - K2M, Inc. - 2021-07-27](https://www.keypedia.com/records/fda_inspections/k2m-inc/454d4a18-9f02-4c82-928b-a4a8335a65a1) — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2021
- [FDA Inspection 1148726 - K2M, Inc. - 2021-07-27](https://www.keypedia.com/records/fda_inspections/k2m-inc/c9dfbd98-0f6b-4549-b1be-6317a8fe2920) — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2021
- [FDA Inspection 1076835 - K2M, Inc. - 2018-12-07](https://www.keypedia.com/records/fda_inspections/k2m-inc/68aaf95f-f6a6-40ef-9a39-10dc958e4c5d) — classification: No Action Indicated (NAI), source: FDA, date: December 7, 2018
- [FDA Inspection 992904 - K2M, Inc. - 2016-11-16](https://www.keypedia.com/records/fda_inspections/k2m-inc/c4c5ce42-ecd4-418c-8dc7-0f046a30700b) — classification: No Action Indicated (NAI), source: FDA, date: November 16, 2016
- [FDA Inspection 992904 - K2M, Inc. - 2016-11-16](https://www.keypedia.com/records/fda_inspections/k2m-inc/99041f68-dd23-47fd-87a8-0b887c646e90) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2016
- [FDA Inspection 967903 - K2M, Inc. - 2016-04-21](https://www.keypedia.com/records/fda_inspections/k2m-inc/71fac753-a8c4-4130-8b9c-f56099078c80) — classification: No Action Indicated (NAI), source: FDA, date: April 21, 2016

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