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Manta Bay S.A. De C.V.

FDA import alert and refusal historyLos Mochis, MexicoFEI 3004291386

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

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As of October 26, 2026, Manta Bay S.A. De C.V. (Los Mochis, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for shrimp; shrimp & prawn aquacultured harvested, published by FDA on September 18, 2009, 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 Manta Bay S.A. De C.V.

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

2009

  1. Import alert listing
    Listed on Import Alert 16-81red listShrimp; Shrimp & Prawn Aquacultured Harvested
    Source

Questions about Manta Bay S.A. De C.V.

Is Manta Bay S.A. De C.V. on an FDA import alert?
Yes. As of October 26, 2026, Manta Bay S.A. De C.V. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for shrimp; shrimp & prawn aquacultured harvested; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Manta Bay S.A. De C.V.?
No FDA import refusals for Manta Bay S.A. De C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Manta Bay S.A. De C.V.'s FEI number?
Manta Bay S.A. De C.V.'s FDA Establishment Identifier (FEI) is 3004291386.
Can shipments from Manta Bay S.A. De C.V. still enter the U.S.?
Shipments of shrimp; shrimp & prawn aquacultured harvested from Manta Bay S.A. De C.V. 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 subjectManta Bay 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.