# FDA Inspection 1282694 - rms Company - September 12, 2025

Source: https://www.keypedia.com/records/fda_inspections/rms-company/28693eba-59c1-47f8-94ce-27b687f89cf1
Source feed: FDA_Inspections

> FDA Inspection 1282694 for rms Company on September 12, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1282694
- Company Name: rms Company
- Inspection Date: 2025-09-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1282694 - 2025-09-12](https://www.keypedia.com/records/fda_inspections/rms-company/0668187d-2655-4e4d-ad4c-a7224a0fbf12)
- [FDA Inspection 1169768 - 2022-05-18](https://www.keypedia.com/records/fda_inspections/rms-company/67d418fe-22b7-48db-b095-8291c3883e89)
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- [FDA Inspection 787337 - 2012-06-20](https://www.keypedia.com/records/fda_inspections/rms-company/dda3b7bb-c656-47c6-82ce-a0df8ac59dd9)
- [FDA Inspection 565675 - 2009-02-27](https://www.keypedia.com/records/fda_inspections/rms-company/84aa1149-e4d3-4d9b-a7fe-b5f8e3ea1474)

Company: https://www.keypedia.com/companies/rms-company/35265af4-630a-4117-a899-d1497aa0adc0

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d