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Biokor

⚠️ Moderate Risk

FEI: 3008315374 • Penza, Penzenskaya obl • RUSSIA

FEI

FEI Number

3008315374

📍

Location

Penza, Penzenskaya obl

🇷🇺

Country

RUSSIA
🏢

Address

ul. Lermontova 3, , Penza, Penzenskaya obl, Russia

Moderate Risk

FDA Import Risk Assessment

28.8
LowModerateHighCritical

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

Statistics

3
Total Refusals
9
Unique Violations
12/18/2017
Latest Refusal
12/18/2017
Earliest Refusal

Score Breakdown

Violation Severity
47.8×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

163×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2183×

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.

23003×

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.

2743×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

3203×

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.

3243×

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)).

33003×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

38633×

PLANT PART

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)(C) of the FD&C Act in that the supplement contains an herb or other botanical described in section 201(ff)(1)(C), and the label or labeling of the supplement fails to identify any part of the plant from which the ingredient is derived.

38643×

NCONTACT

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(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

Refusal History

DateProductViolationsDivision
12/18/2017
54FCY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
16DIRECTIONS
218LIST INGRE
2300DIETARYLBL
274COLOR LBLG
320LACKS FIRM
324NO ENGLISH
3300ALLERGEN
3863PLANT PART
3864NCONTACT
Division of Northern Border Imports (DNBI)
12/18/2017
54FCY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
16DIRECTIONS
218LIST INGRE
2300DIETARYLBL
274COLOR LBLG
320LACKS FIRM
324NO ENGLISH
3300ALLERGEN
3863PLANT PART
3864NCONTACT
Division of Northern Border Imports (DNBI)
12/18/2017
54FCY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
16DIRECTIONS
218LIST INGRE
2300DIETARYLBL
274COLOR LBLG
320LACKS FIRM
324NO ENGLISH
3300ALLERGEN
3863PLANT PART
3864NCONTACT
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Biokor's FDA import refusal history?

Biokor (FEI: 3008315374) has 3 FDA import refusal record(s) in our database, spanning from 12/18/2017 to 12/18/2017.

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. Biokor's FEI number is 3008315374.

What types of violations has Biokor received?

Biokor has been cited for 9 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 Biokor come from?

All FDA import refusal data for Biokor 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.