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Po Dalmoreproduct

FDA import alert and refusal historyVladivostok, RussiaFEI 3004075033

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Example subjectPo Dalmoreproduc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Po Dalmoreproduct (Vladivostok, Russia) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for multiple products (saury blanched in oil; crabmeat; salmon), published by FDA on March 20, 2023, 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 Po Dalmoreproduct

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

2023

  1. Import alert listing
    Listed on Import Alert 99-45red listMultiple products (saury blanched in oil; crabmeat; salmon)
    Source

Questions about Po Dalmoreproduct

Is Po Dalmoreproduct on an FDA import alert?
Yes. As of October 26, 2026, Po Dalmoreproduct is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for multiple products (saury blanched in oil; crabmeat; salmon); FDA published the listing on March 20, 2023.
Has FDA refused shipments from Po Dalmoreproduct?
No FDA import refusals for Po Dalmoreproduct appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Po Dalmoreproduct's FEI number?
Po Dalmoreproduct's FDA Establishment Identifier (FEI) is 3004075033.
Can shipments from Po Dalmoreproduct still enter the U.S.?
Shipments of multiple products (saury blanched in oil; crabmeat; salmon) from Po Dalmoreproduct can be detained without physical examination under Import Alert 99-45; 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 subjectPo Dalmoreproduc 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.