Victor Hugo Ramos Barajas
FDA import alert and refusal historyTecoman, MexicoFEI 3012032117
As of October 26, 2026, Victor Hugo Ramos Barajas is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between November 18, 2016 and November 29, 2016, most often for salmonella (SALMONELLA).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Papaya (papaw) (subtropical and tropical fruit) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Victor Hugo Ramos Barajas
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import refusalRefused, Papaya (papaw) (subtropical and tropical fruit)SALMONELLAEntry 9L9-0121020-8Source
- Import refusalRefused, Papaya (papaw) (subtropical and tropical fruit)SALMONELLAEntry 9L9-0121944-9Source
Refusal charges, in plain English
- SALMONELLA2 refused lines
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Victor Hugo Ramos Barajas
- Is Victor Hugo Ramos Barajas on an FDA import alert?
- No listing for Victor Hugo Ramos Barajas appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Victor Hugo Ramos Barajas?
- Yes. FDA refused 2 shipment lines from Victor Hugo Ramos Barajas between November 18, 2016 and November 29, 2016. The most recent, on November 29, 2016, was papaya (papaw) (subtropical and tropical fruit), charged as SALMONELLA (salmonella).
- Why did FDA refuse Victor Hugo Ramos Barajas's shipments?
- The most frequent charge is SALMONELLA (salmonella, 2 lines).
- What is Victor Hugo Ramos Barajas's FEI number?
- Victor Hugo Ramos Barajas's FDA Establishment Identifier (FEI) is 3012032117.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.