SupplierRadar

Grupo la Florida Mexico, S.A. de C.V.

FDA import alert and refusal historyTlalnepantla, MexicoFEI 3008314142

Recorded by FDA as GRUPO LA FLORIDA MEXICO, S.A. DE C.V.

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As of October 26, 2026, Grupo la Florida Mexico, S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between January 19, 2018 and June 22, 2020, most often for importer not in compliance with fsvp (FSVP VIO).

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

Current status

Import alerts
Not listed
Last import refusal
Berries, jam, jelly, preserves, marmalade, butter and candied, n.e.c. · FSVP VIO
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Grupo la Florida Mexico, S.A. de C.V.

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

2020

  1. Import refusal
    Refused, 4 lines in one entry: Berries, jam, jelly, preserves, marmalade, butter and candied, n.e.c.; Custard, n.e.c. and 1 moreFSVP VIOEntry FM8-2000812-2Show 4 lines
    • Refused, Berries, jam, jelly, preserves, marmalade, butter and candied, n.e.c.FSVP VIOEntry FM8-2000812-2Source
    • Refused, Custard, n.e.c.FSVP VIOEntry FM8-2000812-2Source
    • Refused, Custard, n.e.c.FSVP VIOEntry FM8-2000812-2Source
    • Refused, Cake decoration (without chocolate)FSVP VIOEntry FM8-2000812-2Source
    Source

2018

  1. Import refusal
    Refused, 2 lines in one entry: Fig (subtropical and tropical fruit); Jicama (root & tuber vegetable)NUTRIT LBLNEEDS FCENO PROCESSEntry EU0-0083441-3Show 2 lines
    Source

2012

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

Refusal charges, in plain English

  • FSVP VIO4 refused lines

    Importer not in compliance with FSVP

    The importer of record appeared not to be in compliance with the Foreign Supplier Verification Program requirements of section 805 of the FD&C Act. The charge concerns the importer's program, not a test result on the food.

  • 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.

  • NO PROCESS2 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.

  • 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.

Questions about Grupo la Florida Mexico, S.A. de C.V.

Is Grupo la Florida Mexico, S.A. de C.V. on an FDA import alert?
No listing for Grupo la Florida Mexico, 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 Grupo la Florida Mexico, S.A. de C.V.?
Yes. FDA refused 6 shipment lines from Grupo la Florida Mexico, S.A. de C.V. between January 19, 2018 and June 22, 2020. The most recent, on June 22, 2020, was berries, jam, jelly, preserves, marmalade, butter and candied, n.e.c., charged as FSVP VIO (importer not in compliance with fsvp).
Why did FDA refuse Grupo la Florida Mexico, S.A. de C.V.'s shipments?
The most frequent charges are FSVP VIO (importer not in compliance with fsvp, 4 lines) and NEEDS FCE (processor not registered for canned or acidified foods, 2 lines).
When was Grupo la Florida Mexico, S.A. de C.V. last inspected by FDA?
FDA's most recent inspection of Grupo la Florida Mexico, S.A. de C.V. with a final classification is dated February 22, 2012 and was classified VAI (Voluntary Action Indicated).
What is Grupo la Florida Mexico, S.A. de C.V.'s FEI number?
Grupo la Florida Mexico, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3008314142.

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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.