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Caiman Products S.A. De C.V.

FDA import alert and refusal historyProgreso, MexicoFEI 3008732552

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Example subjectCaiman Products S.A. De C.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Caiman Products S.A. De C.V. is on the green list of FDA Import Alert 16-125, 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 Caiman Products S.A. De C.V.

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

2019

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2011

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

2009

  1. Import alert listing
    Listed on Import Alert 16-125green listGroupers, Vacuum or Modified Atmosphere Packaging; Snapper (Red, Gray, Malabar, etc.), Vacuum or Modified Atmosphere Packaging
    Source

Questions about Caiman Products S.A. De C.V.

Is Caiman Products S.A. De C.V. on an FDA import alert?
Yes. As of October 26, 2026, Caiman Products S.A. De C.V. is on the green list of FDA Import Alert 16-125, “Refrigerated raw fish in reduced oxygen packaging”, for groupers, vacuum or modified atmosphere packaging; snapper (red, gray, malabar, etc.), vacuum or modified atmosphere packaging; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Caiman Products S.A. De C.V.?
No FDA import refusals for Caiman Products S.A. De C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Caiman Products S.A. De C.V. last inspected by FDA?
FDA's most recent inspection of Caiman Products S.A. De C.V. with a final classification is dated September 12, 2019 and was classified VAI (Voluntary Action Indicated).
What is Caiman Products S.A. De C.V.'s FEI number?
Caiman Products S.A. De C.V.'s FDA Establishment Identifier (FEI) is 3008732552.

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Example subjectCaiman Products S.A. De C.V 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.