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Jp Russell Science Ltd

⚠️ Moderate Risk

FEI: 3009903702 • Nicosia • CYPRUS

FEI

FEI Number

3009903702

📍

Location

Nicosia

🇨🇾

Country

CYPRUS
🏢

Address

30 Chytron St Office A 32, , Nicosia, , Cyprus

Moderate Risk

FDA Import Risk Assessment

41.1
LowModerateHighCritical

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

Statistics

20
Total Refusals
10
Unique Violations
1/13/2017
Latest Refusal
2/4/2013
Earliest Refusal

Score Breakdown

Violation Severity
53.4×40%
Refusal Volume
49.0×30%
Recency
0.0×20%
Frequency
50.7×10%
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

212013×

UNSFDIETSP

The article appears to be a dietary supplement or ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.

4826×

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.

3246×

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)).

38644×

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.

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.

36812×

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.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

3201×

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.

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

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).

Refusal History

DateProductViolationsDivision
1/13/2017
54ABE99VITAMIN, N.E.C.
2300DIETARYLBL
324NO ENGLISH
3864NCONTACT
482NUTRIT LBL
New Orleans District Office (NOL-DO)
1/13/2017
54YCE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
324NO ENGLISH
3864NCONTACT
482NUTRIT LBL
New Orleans District Office (NOL-DO)
1/13/2017
54YBE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
324NO ENGLISH
3864NCONTACT
482NUTRIT LBL
New Orleans District Office (NOL-DO)
8/9/2016
52BYY99FOOD RELATED ITEM, N.E.C.
324NO ENGLISH
3864NCONTACT
482NUTRIT LBL
New Orleans District Office (NOL-DO)
9/29/2015
61SAJ99ANTI-ECZEMATIC N.E.C.
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/2/2014
54YBE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2120UNSFDIETSP
Division of Southeast Imports (DSEI)
9/5/2014
54BYE99MINERAL N.E.C.
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
9/5/2014
54YBE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
9/5/2014
53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
9/3/2014
54YBE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2120UNSFDIETSP
324NO ENGLISH
New Orleans District Office (NOL-DO)
8/28/2014
54ABY99VITAMIN, N.E.C.
2120UNSFDIETSP
Division of Southeast Imports (DSEI)
8/28/2014
41GHR01NUTRITIONALLY COMPLETE FORMULATIONS
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
8/20/2014
54AYY99VITAMIN, N.E.C.
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
8/20/2014
54ABE99VITAMIN, N.E.C.
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
8/7/2014
54ABE99VITAMIN, N.E.C.
2120UNSFDIETSP
Division of Southeast Imports (DSEI)
8/7/2014
54ABE99VITAMIN, N.E.C.
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
7/29/2014
54ABE99VITAMIN, N.E.C.
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
7/28/2014
54ABE99VITAMIN, N.E.C.
2120UNSFDIETSP
New Orleans District Office (NOL-DO)
7/10/2014
54YCF99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2120UNSFDIETSP
320LACKS FIRM
324NO ENGLISH
3681NCONTACTS
482NUTRIT LBL
New Orleans District Office (NOL-DO)
2/4/2013
54HBH99FATS AND LIPID SUBSTANCES, N.E.C.
3681NCONTACTS
482NUTRIT LBL
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Jp Russell Science Ltd's FDA import refusal history?

Jp Russell Science Ltd (FEI: 3009903702) has 20 FDA import refusal record(s) in our database, spanning from 2/4/2013 to 1/13/2017.

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. Jp Russell Science Ltd's FEI number is 3009903702.

What types of violations has Jp Russell Science Ltd received?

Jp Russell Science Ltd has been cited for 10 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 Jp Russell Science Ltd come from?

All FDA import refusal data for Jp Russell Science Ltd 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.