# Vicon Motion Systems, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vicon-motion-systems-inc/3bae0cdb-12c4-4676-8a41-74792a18442c

> Inspection records and compliance data for Vicon Motion Systems, Inc. in Centennial, Colorado. Access full analysis and detailed observations.

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## Details

- Name: Vicon Motion Systems, Inc.
- FEI Number: 1000377231
- City: Centennial
- State: Colorado
- Country Name: United States
- Address Line 1: 7388 S Revere Pkwy Ste 901
- Zip Code: 80112

## Related Documents

- [FDA Inspection 1038632 - Vicon Motion Systems, Inc. - 2017-12-21](https://www.globalkeysolutions.net/records/fda_inspections/vicon-motion-systems-inc/183165c5-027e-4ef6-af37-eec6d9e8c628) — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2017
- [FDA Inspection 1038632 - Vicon Motion Systems, Inc. - 2017-12-21](https://www.globalkeysolutions.net/records/fda_inspections/vicon-motion-systems-inc/8c75d11c-f157-4c6e-a29e-c4449d4c567b) — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2017
- [FDA Inspection 836303 - Vicon Motion Systems, Inc. - 2013-06-11](https://www.globalkeysolutions.net/records/fda_inspections/vicon-motion-systems-inc/9cfcf890-09dc-4847-bc35-7fef3bb257d9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 11, 2013
- [FDA Inspection 836303 - Vicon Motion Systems, Inc. - 2013-06-11](https://www.globalkeysolutions.net/records/fda_inspections/vicon-motion-systems-inc/9c064287-f889-4c46-b6f8-eca22ee931d3) — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2013
- [FDA Inspection 614966 - Vicon Motion Systems, Inc. - 2009-09-22](https://www.globalkeysolutions.net/records/fda_inspections/vicon-motion-systems-inc/8e38fe98-9e6c-486a-bd7f-422fdecb6b1a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 22, 2009
- [FDA Inspection 614966 - Vicon Motion Systems, Inc. - 2009-09-22](https://www.globalkeysolutions.net/records/fda_inspections/vicon-motion-systems-inc/161018ee-32ba-438c-84b0-a41742ea3503) — classification: No Action Indicated (NAI), source: FDA, date: September 22, 2009

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