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Agroindustrias Deandar de Delicias S.A. de C.V.

FDA import alert and refusal historyDelicias, MexicoFEI 3004291571

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Example subjectAgroindustrias Deandar de Delicias S.A. de C.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Agroindustrias Deandar de Delicias S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines between January 6, 2017 and August 24, 2021, most often for no scheduled process filed (NO PROCESS).

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

Current status

Import alerts
Not listed
Last import refusal
Jalapeno pepper, hot (fruit used as vegetable) · NO PROCESS
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Agroindustrias Deandar de Delicias S.A. de C.V.

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

2021

  1. Import refusal
    Refused, Jalapeno pepper, hot (fruit used as vegetable)NO PROCESSEntry EHJ-0055468-0
    Source

2018

  1. Import refusal
    Refused, Pepper sauce (hot, mild, etc.)NO PROCESSEntry EHJ-0039494-7
    Source

2017

  1. Import refusal
    Refused, Cucumbers (fruit used as vegetable)PESTICIDEEntry EHJ-0036480-9
    Source
  2. Import refusal
    Refused, Cucumbers (fruit used as vegetable)PESTICIDEEntry EHJ-0036425-4
    Source
  3. Import refusal
    Refused, Jalapeno pepper, hot (fruit used as vegetable)NO PROCESSEntry EHJ-0035882-7
    Source
  4. Import refusal
    Refused, Jalapeno pepper, hot (fruit used as vegetable)NO PROCESSEntry EHJ-0035297-8
    Source
  5. Import refusal
    Refused, Husk tomato (tomatillo) (fruit used as vegetable)LIST INGREEntry EHJ-0034534-5
    Source

2011

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • NO PROCESS4 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.

  • 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.

  • LIST INGRE1 refused line

    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 Agroindustrias Deandar de Delicias S.A. de C.V.

Is Agroindustrias Deandar de Delicias S.A. de C.V. on an FDA import alert?
No listing for Agroindustrias Deandar de Delicias 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 Agroindustrias Deandar de Delicias S.A. de C.V.?
Yes. FDA refused 7 shipment lines from Agroindustrias Deandar de Delicias S.A. de C.V. between January 6, 2017 and August 24, 2021. The most recent, on August 24, 2021, was jalapeno pepper, hot (fruit used as vegetable), charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Agroindustrias Deandar de Delicias S.A. de C.V.'s shipments?
The most frequent charges are NO PROCESS (no scheduled process filed, 4 lines) and PESTICIDE (pesticide chemical residue, 2 lines).
When was Agroindustrias Deandar de Delicias S.A. de C.V. last inspected by FDA?
FDA's most recent inspection of Agroindustrias Deandar de Delicias S.A. de C.V. with a final classification is dated July 1, 2011 and was classified NAI (No Action Indicated).
What is Agroindustrias Deandar de Delicias S.A. de C.V.'s FEI number?
Agroindustrias Deandar de Delicias S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3004291571.

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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.