Gabriela Ramos Evaristo
FDA import alert and refusal historyCoyuca De Benitez, MexicoFEI 3045218436
Recorded by FDA as GABRIELA RAMOS EVARISTO
As of October 26, 2026, Gabriela Ramos Evaristo is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on August 6, 2026, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Caramel candy pieces, hard, with fruit (without chocolate) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Gabriela Ramos Evaristo
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalSource
Refused, 2 lines in one entry: Caramel candy pieces, hard, with fruit (without chocolate)FILTHYEntry SCS-9330063-7Show 2 linesHide lines
Refusal charges, in plain English
- FILTHY2 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Gabriela Ramos Evaristo
- Is Gabriela Ramos Evaristo on an FDA import alert?
- No listing for Gabriela Ramos Evaristo 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 Gabriela Ramos Evaristo?
- Yes. FDA refused 2 shipment lines from Gabriela Ramos Evaristo on August 6, 2026. The most recent, on August 6, 2026, was caramel candy pieces, hard, with fruit (without chocolate), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Gabriela Ramos Evaristo's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- What is Gabriela Ramos Evaristo's FEI number?
- Gabriela Ramos Evaristo's FDA Establishment Identifier (FEI) is 3045218436.
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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.