# FDA 483 - VEOS USA, Inc. - September 03, 2025

Source: https://www.keypedia.com/records/483/veos-usa-inc/e749cffe-e5e3-4a85-8a8a-08349e377335

> FDA 483 for VEOS USA, Inc. on September 03, 2025. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: VEOS USA, Inc.
- Inspection Date: 2025-09-03
- Product Type: other
- Office Name: Detroit District Office
- Summary: An FDA inspection of VEOS USA, Inc. in Adrian, MI, a manufacturer of egg products, revealed significant deficiencies in preventive controls and environmental monitoring. The firm failed to adequately pasteurize liquid raw egg ingredients to control Salmonella and Enterobacteriaceae, and did not maintain proper environmental monitoring or temperature controls for raw egg storage. These issues indicate a high potential for product contamination and include a repeat observation regarding preventive controls.

## Related Officers

- [Joseph R. Haynes](https://www.keypedia.com/people/joseph-r-haynes/5ec8c4b4-7a47-40cd-b31a-db41aa35a1d8)

Company: https://www.keypedia.com/companies/veos-usa-inc/40ddedde-1726-4f6c-bd99-6532c431cdb8

Office: https://www.keypedia.com/offices/detroit-district-office/b09a1815-a000-40c0-bb44-5432ce87ed03