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DILYAVER

⚠️ Moderate Risk

FEI: 3006807805 • Zherbinka, Moskovskaya oblast • RUSSIA

FEI

FEI Number

3006807805

📍

Location

Zherbinka, Moskovskaya oblast

🇷🇺

Country

RUSSIA
🏢

Address

Zheleznodorozhnay Street 24, , Zherbinka, Moskovskaya oblast, Russia

Moderate Risk

FDA Import Risk Assessment

31.9
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

7
Total Refusals
3
Unique Violations
4/9/2012
Latest Refusal
12/23/2010
Earliest Refusal

Score Breakdown

Violation Severity
41.1×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
54.0×10%
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

3247×

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)).

621×

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).

831×

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.

Refusal History

DateProductViolationsDivision
4/9/2012
25PCT99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
12/23/2010
09CYY26MILK AND MILK PRODUCTS, CULTURED OR ACIDIFIED
324NO ENGLISH
New York District Office (NYK-DO)
12/23/2010
09CYY26MILK AND MILK PRODUCTS, CULTURED OR ACIDIFIED
324NO ENGLISH
New York District Office (NYK-DO)
12/23/2010
09CYY26MILK AND MILK PRODUCTS, CULTURED OR ACIDIFIED
324NO ENGLISH
New York District Office (NYK-DO)
12/23/2010
09CGY26MILK AND MILK PRODUCTS, CULTURED OR ACIDIFIED
324NO ENGLISH
New York District Office (NYK-DO)
12/23/2010
09CGY26MILK AND MILK PRODUCTS, CULTURED OR ACIDIFIED
324NO ENGLISH
New York District Office (NYK-DO)
12/23/2010
09CGY26MILK AND MILK PRODUCTS, CULTURED OR ACIDIFIED
324NO ENGLISH
New York District Office (NYK-DO)

Frequently Asked Questions

What is DILYAVER's FDA import refusal history?

DILYAVER (FEI: 3006807805) has 7 FDA import refusal record(s) in our database, spanning from 12/23/2010 to 4/9/2012.

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. DILYAVER's FEI number is 3006807805.

What types of violations has DILYAVER received?

DILYAVER has been cited for 3 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 DILYAVER come from?

All FDA import refusal data for DILYAVER 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.