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Jorge Avel Sauceda Garcia

FDA import alert and refusal historyTijuana, MexicoFEI 3010105314

Recorded by FDA as JORGE AVEL SAUCEDA GARCIA

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Example subjectJorge Avel Sauceda Garci added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jorge Avel Sauceda Garcia (Tijuana, Mexico) is on the red list of FDA Import Alert 16-04 (Seafood products that appear to be misbranded) for skate wing; manta ray, published by FDA on August 15, 2013, 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
None on record

Every FDA record for Jorge Avel Sauceda Garcia

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

2013

  1. Import alert listing
    Listed on Import Alert 16-04red listSkate Wing; Manta Ray
    Source

Questions about Jorge Avel Sauceda Garcia

Is Jorge Avel Sauceda Garcia on an FDA import alert?
Yes. As of October 26, 2026, Jorge Avel Sauceda Garcia is on the red list of FDA Import Alert 16-04, “Seafood products that appear to be misbranded”, for skate wing; manta ray; FDA published the listing on August 15, 2013.
Has FDA refused shipments from Jorge Avel Sauceda Garcia?
No FDA import refusals for Jorge Avel Sauceda Garcia appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Jorge Avel Sauceda Garcia's FEI number?
Jorge Avel Sauceda Garcia's FDA Establishment Identifier (FEI) is 3010105314.
Can shipments from Jorge Avel Sauceda Garcia still enter the U.S.?
Shipments of skate wing; manta ray from Jorge Avel Sauceda Garcia can be detained without physical examination under Import Alert 16-04; 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 subjectJorge Avel Sauceda Garci 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.