# Arch - MedTorque Inc. - Inspection Records

Source: https://www.keypedia.com/companies/arch-medtorque-inc/04a497d6-a324-48c7-93eb-57ed1c38ef79

> Inspection records and compliance data for Arch - MedTorque Inc. in Kenosha, Wisconsin. Access full analysis and detailed observations.

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## Details

- Name: Arch - MedTorque Inc.
- FEI Number: 3005874553
- City: Kenosha
- State: Wisconsin
- Country Name: United States
- Address Line 1: 5601 95th Ave
- Zip Code: 53144

## Related Documents

- [483 - Arch - MedTorque Inc. - 2023-12-15](https://www.keypedia.com/records/483/arch-medtorque-inc/bd3552f4-5162-4ac8-8efe-a415934a84ed) — source: FDA, date: December 15, 2023
- [FDA Inspection 1225420 - Arch - MedTorque Inc. - 2023-12-15](https://www.keypedia.com/records/fda_inspections/arch-medtorque-inc/129648da-bef8-4583-a292-2b0651495051) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 15, 2023
- [FDA Inspection 1054772 - Arch - MedTorque Inc. - 2018-05-15](https://www.keypedia.com/records/fda_inspections/arch-medtorque-inc/91d306b6-d1b3-4de8-8b77-f1921b3f6074) — classification: No Action Indicated (NAI), source: FDA, date: May 15, 2018
- [FDA Inspection 1054772 - Arch - MedTorque Inc. - 2018-05-15](https://www.keypedia.com/records/fda_inspections/arch-medtorque-inc/a928be1c-aee9-4449-856f-5dc2fff6f9e8) — classification: No Action Indicated (NAI), source: FDA, date: May 15, 2018
- [FDA Inspection 870654 - Arch - MedTorque Inc. - 2014-03-20](https://www.keypedia.com/records/fda_inspections/arch-medtorque-inc/32854304-83d5-4a4e-968d-3ee8cb94609a) — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2014
- [FDA Inspection 870654 - Arch - MedTorque Inc. - 2014-03-20](https://www.keypedia.com/records/fda_inspections/arch-medtorque-inc/d475b60b-e883-4b51-88a7-206c3851bc42) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 20, 2014
- [FDA Inspection 652628 - Arch - MedTorque Inc. - 2010-03-18](https://www.keypedia.com/records/fda_inspections/arch-medtorque-inc/d182a3fa-b089-4fc9-9eaa-3bc79f56a7e9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2010

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## Related Officers

- [Medical Device Specialist](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)