SupplierRadar

Grupo Industrial Cuadritos Biotek

FDA import alert and refusal historyCelaya, MexicoFEI 3010314414

Recorded by FDA as GRUPO INDUSTRIAL CUADRITOS BIOTEK

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Example subjectGrupo Industrial Cuadritos Biote added to Import Alert 16-129 (red list)

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As of October 26, 2026, Grupo Industrial Cuadritos Biotek is not on any FDA import alert in SupplierRadar's records; FDA refused 9 of its shipment lines between June 23, 2017 and June 17, 2022, most often for food additive unsafe under section 409 (UNSAFE ADD).

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

Current status

Import alerts
Not listed
Last import refusal
Beverage base of non-fruit origin, liquid, n.e.c. · UNSAFE ADD
Last warning letter
None found
Last inspection
None on record

Every FDA record for Grupo Industrial Cuadritos Biotek

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

2022

  1. Import refusal
    Refused, 3 lines in one entry: Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0079701-0Show 3 lines
    • Refused, Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0079701-0Source
    • Refused, Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0079701-0Source
    • Refused, Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0079701-0Source
    Source
  2. Import refusal
    Refused, 3 lines in one entry: Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0079640-0Show 3 lines
    • Refused, Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0079640-0Source
    • Refused, Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0079640-0Source
    • Refused, Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0079640-0Source
    Source
  3. Import refusal
    Refused, 2 lines in one entry: Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0078692-2Show 2 lines
    • Refused, Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0078692-2Source
    • Refused, Beverage base of non-fruit origin, liquid, n.e.c.UNSAFE ADDEntry ANG-0078692-2Source
    Source

2017

  1. Import refusal
    Refused, Cereal preparations not elsewhere mentioned, n.e.c.UNSAFE ADDNUTRIT LBLHEALTH CEntry ANG-0045939-7
    Source

Refusal charges, in plain English

  • UNSAFE ADD9 refused lines

    Food additive unsafe under section 409

    The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

  • HEALTH C1 refused line

    Unauthorized nutrient content or health claim

    The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

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

Questions about Grupo Industrial Cuadritos Biotek

Is Grupo Industrial Cuadritos Biotek on an FDA import alert?
No listing for Grupo Industrial Cuadritos Biotek 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 Grupo Industrial Cuadritos Biotek?
Yes. FDA refused 9 shipment lines from Grupo Industrial Cuadritos Biotek between June 23, 2017 and June 17, 2022. The most recent, on June 17, 2022, was beverage base of non-fruit origin, liquid, n.e.c., charged as UNSAFE ADD (food additive unsafe under section 409).
Why did FDA refuse Grupo Industrial Cuadritos Biotek's shipments?
The most frequent charges are UNSAFE ADD (food additive unsafe under section 409, 9 lines) and HEALTH C (unauthorized nutrient content or health claim, 1 line).
What is Grupo Industrial Cuadritos Biotek's FEI number?
Grupo Industrial Cuadritos Biotek's FDA Establishment Identifier (FEI) is 3010314414.

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Example subjectGrupo Industrial Cuadritos Biote 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.