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Canco Limited

FDA import alert and refusal historySeaforth, JamaicaFEI 3004267007

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Example subjectCanco Limite added to Import Alert 16-129 (red list)

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As of October 26, 2026, Canco Limited is on the green list of FDA Import Alert 21-11, 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 VAI (Voluntary Action Indicated)

Every FDA record for Canco Limited

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

2023

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

2012

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2009

  1. Import alert listing
    Listed on Import Alert 21-11green listAckees (Subtropical and Tropical Fruit), Metal, Commercially Sterile
    Source

Questions about Canco Limited

Is Canco Limited on an FDA import alert?
Yes. As of October 26, 2026, Canco Limited is on the green list of FDA Import Alert 21-11, “Ackees Due to Hypoglycin A”, for ackees (subtropical and tropical fruit), metal, commercially sterile; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Canco Limited?
No FDA import refusals for Canco Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Canco Limited last inspected by FDA?
FDA's most recent inspection of Canco Limited with a final classification is dated January 17, 2023 and was classified VAI (Voluntary Action Indicated).
What is Canco Limited's FEI number?
Canco Limited's FDA Establishment Identifier (FEI) is 3004267007.

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Example subjectCanco Limite 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.