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TWINS TEC

⚠️ Moderate Risk

FEI: 3013727199 • Moscow, Moscow g • RUSSIA

FEI

FEI Number

3013727199

📍

Location

Moscow, Moscow g

🇷🇺

Country

RUSSIA
🏢

Address

Ul. Ryabinovaya 65, , Moscow, Moscow g, Russia

Moderate Risk

FDA Import Risk Assessment

30.4
LowModerateHighCritical

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

Statistics

4
Total Refusals
16
Unique Violations
7/10/2018
Latest Refusal
6/26/2018
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

4734×

LABELING

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

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.

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.

4823×

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.

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)).

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.

33003×

ALLERGEN

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

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.

2743×

COLOR LBLG

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

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.

38623×

DIETARYING

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)(A) of the FD&C Act in that the dietary supplement label or labeling fails to list the name of each dietary ingredient of the supplement and the quantity of each such dietary ingredient or , with respect to a proprietary blend of such dietary ingredients, the total quantity of all dietary ingredients in the blend.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

3351×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

4721×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

Refusal History

DateProductViolationsDivision
7/10/2018
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
16DIRECTIONS
218LIST INGRE
274COLOR LBLG
320LACKS FIRM
324NO ENGLISH
3300ALLERGEN
3862DIETARYING
3863PLANT PART
3864NCONTACT
473LABELING
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
7/10/2018
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
16DIRECTIONS
218LIST INGRE
274COLOR LBLG
320LACKS FIRM
324NO ENGLISH
3300ALLERGEN
3862DIETARYING
3863PLANT PART
3864NCONTACT
473LABELING
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
6/26/2018
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
335LACKS N/C
472NO ENGLISH
473LABELING
Division of Northern Border Imports (DNBI)
6/26/2018
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
16DIRECTIONS
218LIST INGRE
274COLOR LBLG
320LACKS FIRM
324NO ENGLISH
3300ALLERGEN
3862DIETARYING
3863PLANT PART
3864NCONTACT
473LABELING
482NUTRIT LBL
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is TWINS TEC's FDA import refusal history?

TWINS TEC (FEI: 3013727199) has 4 FDA import refusal record(s) in our database, spanning from 6/26/2018 to 7/10/2018.

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. TWINS TEC's FEI number is 3013727199.

What types of violations has TWINS TEC received?

TWINS TEC has been cited for 16 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 TWINS TEC come from?

All FDA import refusal data for TWINS TEC 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.