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OOO Gustera-2 Pkf

FDA import alert and refusal historyAstrakhan, RussiaFEI 3010759572

Recorded by FDA as OOO GUSTERA-2 PKF

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Example subjectOOO Gustera-2 Pk added to Import Alert 16-129 (red list)

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As of October 26, 2026, OOO Gustera-2 Pkf (Astrakhan, Russia) is on the red list of FDA Import Alert 16-119 (Fish products from importer and processor combinations) for dried; vacuum-packed taran (caspian) roach, published by FDA on January 21, 2015, 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 OOO Gustera-2 Pkf

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

2015

  1. Import alert listing
    Listed on Import Alert 16-119red listDried; Vacuum-packed Taran (Caspian) Roach
    Source

Questions about OOO Gustera-2 Pkf

Is OOO Gustera-2 Pkf on an FDA import alert?
Yes. As of October 26, 2026, OOO Gustera-2 Pkf is on the red list of FDA Import Alert 16-119, “Fish products from importer and processor combinations”, for dried; vacuum-packed taran (caspian) roach; FDA published the listing on January 21, 2015.
Has FDA refused shipments from OOO Gustera-2 Pkf?
No FDA import refusals for OOO Gustera-2 Pkf appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is OOO Gustera-2 Pkf's FEI number?
OOO Gustera-2 Pkf's FDA Establishment Identifier (FEI) is 3010759572.
Can shipments from OOO Gustera-2 Pkf still enter the U.S.?
Shipments of dried; vacuum-packed taran (caspian) roach from OOO Gustera-2 Pkf can be detained without physical examination under Import Alert 16-119; 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 subjectOOO Gustera-2 Pk 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.