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Gelagri SAS

FDA import alert and refusal historyLanderneau Cedex, FranceFEI 3012234227

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Example subjectGelagri SA added to Import Alert 16-129 (red list)

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As of October 25, 2026, Gelagri SAS is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between December 7, 2018 and January 21, 2020, most often for pesticide chemical residue (PESTICIDE).

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

Current status

Import alerts
Not listed
Last import refusal
Stringbeans · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Gelagri SAS

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

2020

  1. Import refusal
    Refused, StringbeansPESTICIDEEntry 442-8820469-4
    Source

2018

  1. Import refusal
    Refused, StringbeansPESTICIDEEntry 442-8206161-1
    Source

Refusal charges, in plain English

  • PESTICIDE2 refused lines

    Pesticide chemical residue

    The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

Questions about Gelagri SAS

Is Gelagri SAS on an FDA import alert?
No listing for Gelagri SAS appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the France page.
Has FDA refused shipments from Gelagri SAS?
Yes. FDA refused 2 shipment lines from Gelagri SAS between December 7, 2018 and January 21, 2020. The most recent, on January 21, 2020, was stringbeans, charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse Gelagri SAS's shipments?
The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
What is Gelagri SAS's FEI number?
Gelagri SAS's FDA Establishment Identifier (FEI) is 3012234227.

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Example subjectGelagri SA 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.