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Diveevo

⚠️ Moderate Risk

FEI: 3010028660 • Salkovo Village • RUSSIA

FEI

FEI Number

3010028660

📍

Location

Salkovo Village

🇷🇺

Country

RUSSIA
🏢

Address

5 Podolskiy Area Kurganski Area, , Salkovo Village, , Russia

Moderate Risk

FDA Import Risk Assessment

35.3
LowModerateHighCritical

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

Statistics

9
Total Refusals
8
Unique Violations
10/10/2014
Latest Refusal
10/10/2014
Earliest Refusal

Score Breakdown

Violation Severity
38.1×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
90.0×10%
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

4828×

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.

23008×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

2188×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3208×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

3248×

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)).

36818×

NCONTACTS

The product is a dietary supplement that is marketed in the United States and appears to not have a domestic address or domestic phone number through which the responsible person may receive a report of a serious adverse event.

4738×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

2381×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

Refusal History

DateProductViolationsDivision
10/10/2014
45VH99NUTRITIVE SWEETNERS (FOOD ADDITIVES FOR HUMAN USE)
238UNSAFE ADD
Division of Northeast Imports (DNEI)
10/10/2014
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
324NO ENGLISH
3681NCONTACTS
473LABELING
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/10/2014
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
324NO ENGLISH
3681NCONTACTS
473LABELING
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/10/2014
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
324NO ENGLISH
3681NCONTACTS
473LABELING
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/10/2014
54KBA03VALERIAN (HERBAL & BOTANICALS, NOT TEAS II)
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
324NO ENGLISH
3681NCONTACTS
473LABELING
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/10/2014
54FYT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
324NO ENGLISH
3681NCONTACTS
473LABELING
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/10/2014
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
324NO ENGLISH
3681NCONTACTS
473LABELING
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/10/2014
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
324NO ENGLISH
3681NCONTACTS
473LABELING
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/10/2014
54FCK21ROSE HIPS (HERBAL & BOTANICALS, NOT TEAS - IF TEA FORM SEE 31P)
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
324NO ENGLISH
3681NCONTACTS
473LABELING
482NUTRIT LBL
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Diveevo's FDA import refusal history?

Diveevo (FEI: 3010028660) has 9 FDA import refusal record(s) in our database, spanning from 10/10/2014 to 10/10/2014.

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. Diveevo's FEI number is 3010028660.

What types of violations has Diveevo received?

Diveevo has been cited for 8 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 Diveevo come from?

All FDA import refusal data for Diveevo 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.