Hugo Ernesto Arevalo Martinez
FDA import alert and refusal historyTonala, MexicoFEI 3011545248
As of October 26, 2026, Hugo Ernesto Arevalo Martinez is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines on February 25, 2026, most often for importer not in compliance with fsvp (FSVP VIO).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Tortillas · FSVP VIO
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hugo Ernesto Arevalo Martinez
5 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalSource
Refused, 5 lines in one entry: TortillasFSVP VIOEntry GR9-9122677-4Show 5 linesHide lines
Refusal charges, in plain English
- FSVP VIO5 refused lines
Importer not in compliance with FSVP
The importer of record appeared not to be in compliance with the Foreign Supplier Verification Program requirements of section 805 of the FD&C Act. The charge concerns the importer's program, not a test result on the food.
Questions about Hugo Ernesto Arevalo Martinez
- Is Hugo Ernesto Arevalo Martinez on an FDA import alert?
- No listing for Hugo Ernesto Arevalo Martinez 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 Hugo Ernesto Arevalo Martinez?
- Yes. FDA refused 5 shipment lines from Hugo Ernesto Arevalo Martinez on February 25, 2026. The most recent, on February 25, 2026, was tortillas, charged as FSVP VIO (importer not in compliance with fsvp).
- Why did FDA refuse Hugo Ernesto Arevalo Martinez's shipments?
- The most frequent charge is FSVP VIO (importer not in compliance with fsvp, 5 lines).
- What is Hugo Ernesto Arevalo Martinez's FEI number?
- Hugo Ernesto Arevalo Martinez's FDA Establishment Identifier (FEI) is 3011545248.
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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.