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Company Stingray

FDA import alert and refusal historyZaporozhye, UkraineFEI 3015082667

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Example subjectCompany Stingra added to Import Alert 16-129 (red list)

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As of October 26, 2026, Company Stingray (Zaporozhye, Ukraine) is on the red list of FDA Import Alert 16-74 (Uneviscerated salt-cured, dried, smoked or fermented fish) for dried bream, published by FDA on February 14, 2020, and has 8 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Bream · MFR INSAN
Last warning letter
None found
Last inspection
None on record

Every FDA record for Company Stingray

9 records, newest first. Each line links to the FDA page it came from.

2025

  1. Import refusal
    Refused, 3 lines in one entry: BreamMFR INSANEntry 9AJ-0007674-8Show 3 lines
    Source

2023

  1. Import refusal
    Refused, BreamMFR INSANEntry 521-0099328-7
    Source

2021

  1. Import refusal
    Refused, 3 lines in one entry: Fish roe, fishery products, n.e.c.INSANITARYNEEDS FCENO PROCESSEntry 521-0096208-4Show 3 lines
    Source

2020

  1. Import alert listing
    Listed on Import Alert 16-74red listDried Bream
    Source

2019

  1. Import refusal
    Refused, BreamFILTHYMFR INSANLACKS N/CEntry 521-0090854-1
    Source

Refusal charges, in plain English

  • MFR INSAN5 refused lines

    Insanitary manufacturing, processing or packing

    The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

  • INSANITARY3 refused lines

    Prepared, packed or held under insanitary conditions

    The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth or rendered injurious to health.

  • NEEDS FCE3 refused lines

    Processor not registered for canned or acidified foods

    The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

  • NO PROCESS3 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

  • LACKS N/C1 refused line

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

Questions about Company Stingray

Is Company Stingray on an FDA import alert?
Yes. As of October 26, 2026, Company Stingray is on the red list of FDA Import Alert 16-74, “Uneviscerated salt-cured, dried, smoked or fermented fish”, for dried bream; FDA published the listing on February 14, 2020.
Has FDA refused shipments from Company Stingray?
Yes. FDA refused 8 shipment lines from Company Stingray between December 16, 2019 and October 15, 2025. The most recent, on October 15, 2025, was bream, charged as MFR INSAN (insanitary manufacturing, processing or packing).
Why did FDA refuse Company Stingray's shipments?
The most frequent charges are MFR INSAN (insanitary manufacturing, processing or packing, 5 lines) and INSANITARY (prepared, packed or held under insanitary conditions, 3 lines).
What is Company Stingray's FEI number?
Company Stingray's FDA Establishment Identifier (FEI) is 3015082667.
Can shipments from Company Stingray still enter the U.S.?
Shipments of dried bream from Company Stingray can be detained without physical examination under Import Alert 16-74; 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 subjectCompany Stingra 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.