# Wright Medical Technology, Inc. - District Service Center - St. Louis, Fenton, MO – FDA Inspections

Source: https://www.keypedia.com/companies/wright-medical-technology-inc-district-service-center-st-louis/c28aadac-d9d2-46c8-997a-a4c90cfa58d6

> Inspection records and compliance data for Wright Medical Technology, Inc. - District Service Center - St. Louis in Fenton, Missouri. 4 FDA inspections on record, last inspected June 14, 2022.

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## Details

- Name: Wright Medical Technology, Inc. - District Service Center - St. Louis
- FEI Number: 3005956797
- Address Line 1: 1854 Larkin Williams Rd
- City: Fenton
- State: Missouri
- Zip Code: 63026
- Country Name: United States
- Address: 1854 Larkin Williams Rd, Fenton, Missouri 63026, United States
- Country: United States

## Related Documents

- FDA Inspection 1173188 - Wright Medical Technology, Inc. - District Service Center - St. Louis - 2022-06-14 — classification: No Action Indicated (NAI), source: FDA, date: June 14, 2022
- FDA Inspection 1173188 - Wright Medical Technology, Inc. - District Service Center - St. Louis - 2022-06-14 — classification: No Action Indicated (NAI), source: FDA, date: June 14, 2022
- FDA Inspection 1015147 - Wright Medical Technology, Inc. - District Service Center - St. Louis - 2017-05-23 — classification: No Action Indicated (NAI), source: FDA, date: May 23, 2017
- FDA Inspection 1015147 - Wright Medical Technology, Inc. - District Service Center - St. Louis - 2017-05-23 — classification: No Action Indicated (NAI), source: FDA, date: May 23, 2017
- [FDA Inspection 912469 - Wright Medical Technology, Inc. - District Service Center - St. Louis - 2015-02-04](https://www.keypedia.com/records/fda_inspections/wright-medical-technology-inc-district-service-center-st-louis/17ae6e85-3439-4f17-95d7-0c89b112dbb3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 4, 2015
- FDA Inspection 857062 - Wright Medical Technology, Inc. - District Service Center - St. Louis - 2013-11-27 — classification: No Action Indicated (NAI), source: FDA, date: November 27, 2013

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