SupplierRadar

Genoma Lab International S.A. Dec.V.

FDA import alert and refusal historyCiudad De Mexico, MexicoFEI 3014640908

Recorded by FDA as GENOMA LAB INTERNATIONAL S.A. DEC.V.

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Example subjectGenoma Lab International S.A. Dec.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Genoma Lab International S.A. Dec.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 8 of its shipment lines between October 17, 2023 and August 13, 2025, most often for required label information not in english (NO ENGLISH).

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

Current status

Import alerts
Not listed
Last import refusal
Oral rehydration products · UNSAFE COL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Genoma Lab International S.A. Dec.V.

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

2025

  1. Import refusal
    Refused, 7 lines in one entry: Oral rehydration productsUNSAFE COLLIST INGREINCONSPICULACKS FIRMEntry BJG-0197072-1Show 7 lines
    Source

2023

  1. Import refusal
    Refused, Nonalcoholic beverages, n.e.c.FALSENO ENGLISHNUTRIT LBLUNAPPROVEDEntry NDA-0002621-7
    Source

Refusal charges, in plain English

  • NO ENGLISH8 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • NUTRIT LBL8 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • INCONSPICU7 refused lines

    Required information not conspicuous

    Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.

  • LACKS FIRM7 refused lines

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • LIST INGRE7 refused lines

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

  • USUAL NAME7 refused lines

    Common or usual name missing

    The label appeared not to show the common or usual name of the food.

  • UNSAFE COL5 refused lines

    Color additive unsafe under section 721

    The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

  • FALSE1 refused line

    False or misleading labeling

    The labeling appeared to be false or misleading in some particular.

Questions about Genoma Lab International S.A. Dec.V.

Is Genoma Lab International S.A. Dec.V. on an FDA import alert?
No listing for Genoma Lab International S.A. Dec.V. 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 Genoma Lab International S.A. Dec.V.?
Yes. FDA refused 8 shipment lines from Genoma Lab International S.A. Dec.V. between October 17, 2023 and August 13, 2025. The most recent, on August 13, 2025, was oral rehydration products, charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Genoma Lab International S.A. Dec.V.'s shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 8 lines) and NUTRIT LBL (nutrition information missing from label, 8 lines).
What is Genoma Lab International S.A. Dec.V.'s FEI number?
Genoma Lab International S.A. Dec.V.'s FDA Establishment Identifier (FEI) is 3014640908.

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Example subjectGenoma Lab International S.A. Dec.V 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.