# FDA Inspection 1054772 - Arch - MedTorque Inc. - May 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/arch-medtorque-inc/a928be1c-aee9-4449-856f-5dc2fff6f9e8
Source feed: FDA_Inspections

> FDA inspection 1054772 of Arch - MedTorque Inc., May 15, 2018. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1054772
- Company Name: Arch - MedTorque Inc.
- Inspection Date: 2018-05-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1225420 - 2023-12-15](https://www.keypedia.com/records/fda_inspections/arch-medtorque-inc/129648da-bef8-4583-a292-2b0651495051)
- 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)

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
