# FDA 483 - R&D Molders, Inc. - March 05, 2026

Source: https://www.keypedia.com/records/483/rd-molders-inc/5954d006-c8ca-495e-8766-0e50a04af1c3

> FDA 483 for R&D Molders, Inc. on March 05, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: R&D Molders, Inc.
- Inspection Date: 2026-03-05
- Product Type: device
- Office Name: Kansas City District Office
- Summary: An FDA inspection of Lomont Molding LLC in Mount Pleasant, IA, a manufacturer of needle sharps containment containers, identified a significant issue regarding their quality management system. The firm was found to be using unvalidated software for critical manufacturing functions, including inventory, production, and corrective actions. This raises concerns about the control and reliability of their manufacturing processes.

## Related Officers

- [Clifford F. Long](https://www.keypedia.com/people/clifford-f-long/846e5a0c-cb7c-421c-86aa-be9fddfbaaba)

Company: https://www.keypedia.com/companies/rd-molders-inc/d0b4ee71-3cbc-4217-ba18-2d60379b753b

Office: https://www.keypedia.com/offices/kansas-city-district-office/cd397ab1-df4e-46f1-ab1c-0f6db9abcf79