OOO RESURS
⚠️ Moderate Risk
FEI: 3009987562 • Uvelskiy, Chelyabinskaya obl • RUSSIA
FEI Number
3009987562
Location
Uvelskiy, Chelyabinskaya obl
Country
RUSSIAAddress
ul. Zheleznodorozhnaya 59, , Uvelskiy, Chelyabinskaya obl, Russia
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
INCONSPICU
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/19/2022 | 02GFT02BUCKWHEAT FLOUR | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 2/26/2021 | 24BGF70LENTILS, DRIED OR PASTE | 83NO PROCESS | Division of West Coast Imports (DWCI) |
| 9/29/2020 | 05ADT99BREAKFAST FOODS READY TO EAT,N.E.C. | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 9/29/2020 | 05ADT99BREAKFAST FOODS READY TO EAT,N.E.C. | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 3/28/2019 | 24AGT10NAVY (WHITE) BEANS, (BAKED BEANS, PORK & BEANS) | Division of West Coast Imports (DWCI) | |
| 8/27/2018 | 02GGT01BARLEY FLOUR | 9SALMONELLA | Division of West Coast Imports (DWCI) |
| 9/23/2014 | 02GGT01BARLEY FLOUR | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 1/16/2014 | 02GDH01BARLEY FLOUR | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
| 9/24/2012 | 02GDT01BARLEY FLOUR | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 9/14/2012 | 02GGT02BUCKWHEAT FLOUR | Division of Northeast Imports (DNEI) | |
| 7/31/2012 | 02GGT01BARLEY FLOUR | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 6/21/2012 | 02GGT02BUCKWHEAT FLOUR | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is OOO RESURS's FDA import refusal history?
OOO RESURS (FEI: 3009987562) has 12 FDA import refusal record(s) in our database, spanning from 6/21/2012 to 7/19/2022.
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. OOO RESURS's FEI number is 3009987562.
What types of violations has OOO RESURS received?
OOO RESURS has been cited for 7 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 OOO RESURS come from?
All FDA import refusal data for OOO RESURS 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.