# FDA 483 - Radiation Products Design,Inc - March 31, 2026

Source: https://www.keypedia.com/records/483/radiation-products-designinc/41b88702-da1a-4ea9-bbff-6a6d1a5f026c

> FDA 483 for Radiation Products Design,Inc on March 31, 2026. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Radiation Products Design,Inc
- Inspection Date: 2026-03-31
- Product Type: other
- Office Name: Minneapolis District Office
- Summary: An FDA inspection of Radiation Products Design, Inc. in Albertville, MN, a manufacturer of medical devices, identified one significant observation. The firm was cited for failing to adequately document processes for risk management in product realization. This indicates a deficiency in their quality system regarding risk assessment and management procedures.

## Related Documents

- [483 - 2026-03-04](https://www.keypedia.com/records/483/radiation-products-designinc/5a47d0f2-f328-4312-8719-142e40854862)

## Related Officers

- [Investigator ](https://www.keypedia.com/people/christina-l-bigham/f3da8e26-4a8c-43a8-8070-349fe4500289)

Company: https://www.keypedia.com/companies/radiation-products-designinc/bf052072-9353-43aa-a28a-712fe41c9c96

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