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Company Stingray

⚠️ High Risk

FEI: 3015082667 • Zaporozhye, UA-23 • UKRAINE

FEI

FEI Number

3015082667

📍

Location

Zaporozhye, UA-23

🇺🇦

Country

UKRAINE
🏢

Address

Skvorcova Street 236, , Zaporozhye, UA-23, Ukraine

High Risk

FDA Import Risk Assessment

61.4
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

8
Total Refusals
6
Unique Violations
10/15/2025
Latest Refusal
12/16/2019
Earliest Refusal

Score Breakdown

Violation Severity
83.1×40%
Refusal Volume
35.3×30%
Recency
80.9×20%
Frequency
13.7×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

3085×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

3063×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

623×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

833×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

3211×

LACKS N/C

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

Refusal History

DateProductViolationsDivision
10/15/2025
16AYY80BREAM
308MFR INSAN
Division of Northeast Imports (DNEI)
10/15/2025
16AYY80BREAM
308MFR INSAN
Division of Northeast Imports (DNEI)
10/15/2025
16AYY80BREAM
308MFR INSAN
Division of Northeast Imports (DNEI)
2/15/2023
16AVH80BREAM
308MFR INSAN
Division of West Coast Imports (DWCI)
11/2/2021
16YCT04FISH ROE, FISHERY PRODUCTS, N.E.C.
306INSANITARY
62NEEDS FCE
83NO PROCESS
Division of West Coast Imports (DWCI)
11/2/2021
16YCT04FISH ROE, FISHERY PRODUCTS, N.E.C.
306INSANITARY
62NEEDS FCE
83NO PROCESS
Division of West Coast Imports (DWCI)
11/2/2021
16YCT04FISH ROE, FISHERY PRODUCTS, N.E.C.
306INSANITARY
62NEEDS FCE
83NO PROCESS
Division of West Coast Imports (DWCI)
12/16/2019
16AVH80BREAM
249FILTHY
308MFR INSAN
321LACKS N/C
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Company Stingray's FDA import refusal history?

Company Stingray (FEI: 3015082667) has 8 FDA import refusal record(s) in our database, spanning from 12/16/2019 to 10/15/2025.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Company Stingray's FEI number is 3015082667.

What types of violations has Company Stingray received?

Company Stingray has been cited for 6 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about Company Stingray come from?

All FDA import refusal data for Company Stingray is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.