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Punta Xen S. C. de R. L.

FDA import alert and refusal historyChampoton, MexicoFEI 3010650996

Recorded by FDA as PUNTA XEN S. C. DE R. L.

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Example subjectPunta Xen S. C. de R. L added to Import Alert 16-129 (red list)

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As of October 26, 2026, Punta Xen S. C. de R. L. (Champoton, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for ladyfish (elops saurus), published by FDA on May 9, 2014, and has no FDA import refusals recorded since October 2016.

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

Current status

Import alerts
IA 16-81 · red list
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Punta Xen S. C. de R. L.

1 record, newest first. Each line links to the FDA page it came from.

2014

  1. Import alert listing
    Listed on Import Alert 16-81red listLadyfish (Elops saurus)
    Source

Questions about Punta Xen S. C. de R. L.

Is Punta Xen S. C. de R. L. on an FDA import alert?
Yes. As of October 26, 2026, Punta Xen S. C. de R. L. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for ladyfish (elops saurus); FDA published the listing on May 9, 2014.
Has FDA refused shipments from Punta Xen S. C. de R. L.?
No FDA import refusals for Punta Xen S. C. de R. L. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Punta Xen S. C. de R. L.'s FEI number?
Punta Xen S. C. de R. L.'s FDA Establishment Identifier (FEI) is 3010650996.
Can shipments from Punta Xen S. C. de R. L. still enter the U.S.?
Shipments of ladyfish (elops saurus) from Punta Xen S. C. de R. L. can be detained without physical examination under Import Alert 16-81; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectPunta Xen S. C. 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.