# Arch Medical Solutions - Seabrook – FDA Inspection, Aug 7, 2017

Source: https://www.keypedia.com/records/fda_inspections/arch-medical-solutions-seabrook/10151b0e-7a7b-4006-b597-c0ab713d8a7b
Source feed: FDA_Inspections

> FDA inspection 1021652 of Arch Medical Solutions - Seabrook, August 07, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021652
- Company Name: Arch Medical Solutions - Seabrook
- Inspection Date: 2017-08-07
- 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: 1

## Related Documents

- [FDA Inspection 1280080 - 2025-08-06](https://www.keypedia.com/records/fda_inspections/arch-medical-solutions-seabrook/fcdfc3ee-61df-468a-878d-301e7c9321fb)
- [FDA Inspection 1164041 - 2022-02-18](https://www.keypedia.com/records/fda_inspections/arch-medical-solutions-seabrook/90885348-9cbb-402a-9865-a1c33390b07a)
- FDA Inspection 948441 - 2015-10-27

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/arch-medical-solutions-seabrook/c7274e7b-cb5b-4557-bb20-46c7f247e540

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