# FDA 483 - Sucden Americas Corp - March 31, 2025

Source: https://www.globalkeysolutions.net/records/483/sucden-americas-corp/b778a3c9-4d38-4053-aac2-3903db312de4

> FDA 483 for Sucden Americas Corp on March 31, 2025. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Sucden Americas Corp
- Inspection Date: 2025-03-31
- Product Type: other
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: Sudden Americas Corp in Miami, FL, was inspected regarding its Foreign Supplier Verification Program (FSVP). The inspection revealed three significant observations, including a lack of written procedures for foreign supplier verification activities, insufficient documentation of verification frequency, and an inadequate hazard analysis that failed to identify a required control. These issues indicate deficiencies in ensuring the safety and compliance of imported food.

## Related Documents

- [483 - 2025-03-31](https://www.globalkeysolutions.net/records/483/sucden-americas-corp/e02ff112-ba44-4ca4-be0e-7a099ba2e502)

## Related Officers

- [Timothy P. Clune](https://www.globalkeysolutions.net/people/timothy-p-clune/685f0d97-088b-4def-915a-e1eb8839dab0)

Company: https://www.globalkeysolutions.net/companies/sucden-americas-corp/7b36c68e-7af1-42ca-81bf-577c902cee0b

Office: https://www.globalkeysolutions.net/offices/office-of-medical-device-and-radiological-health-division-ii/ae9bd439-479a-420d-9dd8-9fe1fc0863d6