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Fabrica de Galletas La Moderna S.A. de C.V.

FDA import alert and refusal historyToluca De Lerdo, MexicoFEI 3004249151

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Example subjectFabrica de Galletas La Moderna S.A. de C.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Fabrica de Galletas La Moderna S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 9 of its shipment lines between September 3, 2025 and September 11, 2025, most often for std qualit (STD QUALIT).

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

Current status

Import alerts
Not listed
Last import refusal
Mixed plain cookies,biscuits and wafers · LIST INGRE
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Fabrica de Galletas La Moderna S.A. de C.V.

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

2025

  1. Import refusal
    Refused, Mixed plain cookies,biscuits and wafersLIST INGRESTD QUALITEntry GH5-0174220-5
    Source
  2. Import refusal
    Refused, 4 lines in one entry: Butter/butter flavored,plain cookies,biscuits and wafers; Mixed filled/iced cookies,biscuits and wafers and 1 moreSTD QUALITNUTRIT LBLEntry GH5-0172701-6Show 4 lines
    Source
  3. Import refusal
    Refused, 2 lines in one entry: Butter/butter flavored,plain cookies,biscuits and wafersSTD QUALITEntry GH5-0171671-2Show 2 lines
    • Refused, Butter/butter flavored,plain cookies,biscuits and wafersSTD QUALITEntry GH5-0171671-2Source
    • Refused, Butter/butter flavored,plain cookies,biscuits and wafersSTD QUALITEntry GH5-0171671-2Source
    Source
  4. Import refusal
    Refused, Butter/butter flavored,plain cookies,biscuits and wafersLIST INGRESTD QUALITNUTRIT LBLEntry GH5-0174220-5
    Source
  5. Import refusal
    Refused, Mixed plain cookies,biscuits and wafersSTD QUALITEntry GH5-0171671-2
    Source

2019

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2010

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • STD QUALIT9 refused lines

    STD QUALIT

  • NUTRIT LBL5 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.

  • LIST INGRE2 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).

Questions about Fabrica de Galletas La Moderna S.A. de C.V.

Is Fabrica de Galletas La Moderna S.A. de C.V. on an FDA import alert?
No listing for Fabrica de Galletas La Moderna 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 Mexico page.
Has FDA refused shipments from Fabrica de Galletas La Moderna S.A. de C.V.?
Yes. FDA refused 9 shipment lines from Fabrica de Galletas La Moderna S.A. de C.V. between September 3, 2025 and September 11, 2025. The most recent, on September 11, 2025, was mixed plain cookies,biscuits and wafers, charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Fabrica de Galletas La Moderna S.A. de C.V.'s shipments?
The most frequent charges are STD QUALIT (std qualit, 9 lines) and NUTRIT LBL (nutrition information missing from label, 5 lines).
When was Fabrica de Galletas La Moderna S.A. de C.V. last inspected by FDA?
FDA's most recent inspection of Fabrica de Galletas La Moderna S.A. de C.V. with a final classification is dated March 8, 2019 and was classified VAI (Voluntary Action Indicated).
What is Fabrica de Galletas La Moderna S.A. de C.V.'s FEI number?
Fabrica de Galletas La Moderna S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3004249151.

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Example subjectFabrica de Galletas La Moderna S.A. de C.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.