# FDA Inspection 1225420 - Arch - MedTorque Inc. - December 15, 2023

Source: https://www.keypedia.com/records/fda_inspections/arch-medtorque-inc/129648da-bef8-4583-a292-2b0651495051
Source feed: FDA_Inspections

> FDA inspection 1225420 of Arch - MedTorque Inc., December 15, 2023. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1225420
- Company Name: Arch - MedTorque Inc.
- Inspection Date: 2023-12-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 1054772 - 2018-05-15
- FDA Inspection 870654 - 2014-03-20
- [FDA Inspection 652628 - 2010-03-18](https://www.keypedia.com/records/fda_inspections/arch-medtorque-inc/d182a3fa-b089-4fc9-9eaa-3bc79f56a7e9)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7