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La Oriental Salted Fish Factory

FDA import alert and refusal historyMaracaibo, VenezuelaFEI 1000180583

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Example subjectLa Oriental Salted Fish Factor added to Import Alert 16-129 (red list)

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As of October 26, 2026, La Oriental Salted Fish Factory (Maracaibo, Venezuela) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for dried corvina, published by FDA on August 11, 2010, 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 La Oriental Salted Fish Factory

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

2010

  1. Import alert listing
    Listed on Import Alert 16-81red listDried corvina
    Source

Questions about La Oriental Salted Fish Factory

Is La Oriental Salted Fish Factory on an FDA import alert?
Yes. As of October 26, 2026, La Oriental Salted Fish Factory is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for dried corvina; FDA published the listing on August 11, 2010.
Has FDA refused shipments from La Oriental Salted Fish Factory?
No FDA import refusals for La Oriental Salted Fish Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is La Oriental Salted Fish Factory's FEI number?
La Oriental Salted Fish Factory's FDA Establishment Identifier (FEI) is 1000180583.
Can shipments from La Oriental Salted Fish Factory still enter the U.S.?
Shipments of dried corvina from La Oriental Salted Fish Factory 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 subjectLa Oriental Salted Fish Factor 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.