SupplierRadar

Solfi El Salvador, S.A. de C.V.

FDA import alert and refusal historyLa Libertad, El SalvadorFEI 3015341868

Recorded by FDA as SOLFI EL SALVADOR, S.A. DE C.V.

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As of October 26, 2026, Solfi El Salvador, S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 22, 2023, 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
Ices, fruit flavored, n.e.c. · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Solfi El Salvador, S.A. de C.V.

1 record, newest first. Each line links to the FDA page it came from.

2023

  1. Import refusal
    Refused, Ices, fruit flavored, n.e.c.FILTHYEntry 8TQ-0149379-8
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    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 Solfi El Salvador, S.A. de C.V.

Is Solfi El Salvador, S.A. de C.V. on an FDA import alert?
No listing for Solfi El Salvador, S.A. de C.V. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the El Salvador page.
Has FDA refused shipments from Solfi El Salvador, S.A. de C.V.?
Yes. FDA refused 1 shipment line from Solfi El Salvador, S.A. de C.V. on June 22, 2023. The most recent, on June 22, 2023, was ices, fruit flavored, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Solfi El Salvador, S.A. de C.V.'s shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Solfi El Salvador, S.A. de C.V.'s FEI number?
Solfi El Salvador, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3015341868.

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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.