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Bimbo, S.A. de C.V. Galletas Gabi

FDA import alert and refusal historyTultitlan, MexicoFEI 3004252583

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Example subjectBimbo, S.A. de C.V. Galletas Gab added to Import Alert 16-129 (red list)

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As of October 26, 2026, Bimbo, S.A. de C.V. Galletas Gabi has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on July 6, 2017, was classified NAI (No Action Indicated).

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

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Bimbo, S.A. de C.V. Galletas Gabi

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

2017

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

2015

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

Questions about Bimbo, S.A. de C.V. Galletas Gabi

Is Bimbo, S.A. de C.V. Galletas Gabi on an FDA import alert?
No listing for Bimbo, S.A. de C.V. Galletas Gabi 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 Bimbo, S.A. de C.V. Galletas Gabi?
No FDA import refusals for Bimbo, S.A. de C.V. Galletas Gabi appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Bimbo, S.A. de C.V. Galletas Gabi last inspected by FDA?
FDA's most recent inspection of Bimbo, S.A. de C.V. Galletas Gabi with a final classification is dated July 6, 2017 and was classified NAI (No Action Indicated).
What is Bimbo, S.A. de C.V. Galletas Gabi's FEI number?
Bimbo, S.A. de C.V. Galletas Gabi's FDA Establishment Identifier (FEI) is 3004252583.

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Example subjectBimbo, S.A. de C.V. Galletas Gab 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.