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Alimenco S.A.

FDA import alert and refusal historyMilagro, SpainFEI 3007369095

Recorded by FDA as ALIMENCO S.A.

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Example subjectAlimenco S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Alimenco S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on July 18, 2017, most often for no scheduled process filed (NO PROCESS).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Beet tops (leaf & stem vegetable) · NO PROCESS
Last warning letter
None found
Last inspection
None on record

Every FDA record for Alimenco S.A.

2 records, newest first. Each line links to the FDA page it came from.

2017

  1. Import refusal
    Refused, 2 lines in one entry: Beet tops (leaf & stem vegetable); Carrot (root & tuber vegetable)NO PROCESSEntry WGB-1705262-9Show 2 lines
    Source

Refusal charges, in plain English

  • NO PROCESS2 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Alimenco S.A.

Is Alimenco S.A. on an FDA import alert?
No listing for Alimenco S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
Has FDA refused shipments from Alimenco S.A.?
Yes. FDA refused 2 shipment lines from Alimenco S.A. on July 18, 2017. The most recent, on July 18, 2017, was beet tops (leaf & stem vegetable), charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Alimenco S.A.'s shipments?
The most frequent charge is NO PROCESS (no scheduled process filed, 2 lines).
What is Alimenco S.A.'s FEI number?
Alimenco S.A.'s FDA Establishment Identifier (FEI) is 3007369095.

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Example subjectAlimenco S.A added to Import Alert 16-129 (red list)

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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.