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Dulces Regionales Tres Reyes S.A. de C.V.

FDA import alert and refusal historyZamora, MexicoFEI 1000323240

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Example subjectDulces Regionales Tres Reyes S.A. de C.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Dulces Regionales Tres Reyes S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines between September 10, 2018 and June 28, 2024, most often for required information not conspicuous (INCONSPICU).

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

Current status

Import alerts
Not listed
Last import refusal
Rennet, n.e.c. · INCONSPICU
Last warning letter
None found
Last inspection
None on record

Every FDA record for Dulces Regionales Tres Reyes S.A. de C.V.

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

2024

  1. Import refusal
    Refused, Rennet, n.e.c.INCONSPICULABELINGNO PROCESSEntry BJG-0171805-4
    Source

2019

  1. Import refusal
    Refused, Milk and milk products, cultured or acidifiedINCONSPICUNEEDS ACIDNUTRIT LBLNEEDS FCENO PROCESSEntry BJG-0078297-8
    Source
  2. Import refusal
    Refused, Milk and milk products, cultured or acidifiedINCONSPICUNEEDS ACIDNUTRIT LBLNEEDS FCENO PROCESSEntry BJG-0078189-7
    Source
  3. Import refusal
    Refused, Milk and milk products, cultured or acidifiedINSANITARYNEEDS ACIDEntry B2B-0014902-3
    Source

2018

  1. Import refusal
    Refused, Milk and milk products, cultured or acidifiedUNDER PRCEntry ANG-0064403-0
    Source

Refusal charges, in plain English

  • INCONSPICU3 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.

  • NEEDS ACID3 refused lines

    NEEDS ACID

  • NO PROCESS3 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.

  • NEEDS FCE2 refused lines

    Processor not registered for canned or acidified foods

    The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

  • NUTRIT LBL2 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.

  • INSANITARY1 refused line

    Prepared, packed or held under insanitary conditions

    The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth or rendered injurious to health.

  • LABELING1 refused line

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • UNDER PRC1 refused line

    UNDER PRC

Questions about Dulces Regionales Tres Reyes S.A. de C.V.

Is Dulces Regionales Tres Reyes S.A. de C.V. on an FDA import alert?
No listing for Dulces Regionales Tres Reyes 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 Dulces Regionales Tres Reyes S.A. de C.V.?
Yes. FDA refused 5 shipment lines from Dulces Regionales Tres Reyes S.A. de C.V. between September 10, 2018 and June 28, 2024. The most recent, on June 28, 2024, was rennet, n.e.c., charged as INCONSPICU (required information not conspicuous).
Why did FDA refuse Dulces Regionales Tres Reyes S.A. de C.V.'s shipments?
The most frequent charges are INCONSPICU (required information not conspicuous, 3 lines) and NEEDS ACID (needs acid, 3 lines).
What is Dulces Regionales Tres Reyes S.A. de C.V.'s FEI number?
Dulces Regionales Tres Reyes S.A. de C.V.'s FDA Establishment Identifier (FEI) is 1000323240.

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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.