SupplierRadar

Anjari Exportadora S.p.A.

FDA import alert and refusal historySan Sebastian Los Andes, ChileFEI 3014616251

Recorded by FDA as ANJARI EXPORTADORA SPA

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Example subjectAnjari Exportadora S.p.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Anjari Exportadora S.p.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 27, 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
Raisins (dried grapes) (berry) · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Anjari Exportadora S.p.A.

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

2026

  1. Import refusal
    Refused, Raisins (dried grapes) (berry)FILTHYEntry DP4-1016016-3
    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 Anjari Exportadora S.p.A.

Is Anjari Exportadora S.p.A. on an FDA import alert?
No listing for Anjari Exportadora S.p.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Chile page.
Has FDA refused shipments from Anjari Exportadora S.p.A.?
Yes. FDA refused 1 shipment line from Anjari Exportadora S.p.A. on February 27, 2026. The most recent, on February 27, 2026, was raisins (dried grapes) (berry), charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Anjari Exportadora S.p.A.'s shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Anjari Exportadora S.p.A.'s FEI number?
Anjari Exportadora S.p.A.'s FDA Establishment Identifier (FEI) is 3014616251.

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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.