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Guadalupe De Guaymas, S.P.R. De R.L.

FDA import alert and refusal historyGuaymas, MexicoFEI 3000976900

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Example subjectGuadalupe De Guaymas, S.P.R. De R.L added to Import Alert 16-129 (red list)

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As of October 27, 2026, Guadalupe De Guaymas, S.P.R. De R.L. is on the green list of FDA Import Alert 22-01, which exempts its listed products from detention without physical examination under that alert, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Guadalupe De Guaymas, S.P.R. De R.L.

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

2013

  1. Import alert listing
    Listed on Import Alert 22-01green listCantaloupes
    Source

2010

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

Questions about Guadalupe De Guaymas, S.P.R. De R.L.

Is Guadalupe De Guaymas, S.P.R. De R.L. on an FDA import alert?
Yes. As of October 27, 2026, Guadalupe De Guaymas, S.P.R. De R.L. is on the green list of FDA Import Alert 22-01, “Cantaloupes from Mexico”, for cantaloupes; FDA published the listing on April 17, 2013.
Has FDA refused shipments from Guadalupe De Guaymas, S.P.R. De R.L.?
No FDA import refusals for Guadalupe De Guaymas, S.P.R. De R.L. appear in FDA's refusal data since October 2016, as of October 27, 2026.
When was Guadalupe De Guaymas, S.P.R. De R.L. last inspected by FDA?
FDA's most recent inspection of Guadalupe De Guaymas, S.P.R. De R.L. with a final classification is dated October 29, 2010 and was classified NAI (No Action Indicated).
What is Guadalupe De Guaymas, S.P.R. De R.L.'s FEI number?
Guadalupe De Guaymas, S.P.R. De R.L.'s FDA Establishment Identifier (FEI) is 3000976900.

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Example subjectGuadalupe De Guaymas, S.P.R. De R.L 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.