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Unidad De Produccion Paso Limon

FDA import alert and refusal historyPueblo Manlio Fabio Altamirano, MexicoFEI 3010256223

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Example subjectUnidad De Produccion Paso Limo added to Import Alert 16-129 (red list)

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As of October 26, 2026, Unidad De Produccion Paso Limon is on the green list of FDA Import Alert 21-17, 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 Unidad De Produccion Paso Limon

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

2019

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

2012

  1. Import alert listing
    Listed on Import Alert 21-17green listPapaya
    Source

Questions about Unidad De Produccion Paso Limon

Is Unidad De Produccion Paso Limon on an FDA import alert?
Yes. As of October 26, 2026, Unidad De Produccion Paso Limon is on the green list of FDA Import Alert 21-17, “Papaya from Mexico”, for papaya; FDA published the listing on January 4, 2012.
Has FDA refused shipments from Unidad De Produccion Paso Limon?
No FDA import refusals for Unidad De Produccion Paso Limon appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Unidad De Produccion Paso Limon last inspected by FDA?
FDA's most recent inspection of Unidad De Produccion Paso Limon with a final classification is dated June 7, 2019 and was classified NAI (No Action Indicated).
What is Unidad De Produccion Paso Limon's FEI number?
Unidad De Produccion Paso Limon's FDA Establishment Identifier (FEI) is 3010256223.

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Example subjectUnidad De Produccion Paso Limo 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.