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Kore Koncepts

⚠️ Moderate Risk

FEI: 3009537385 • New Delhi, Delhi • INDIA

FEI

FEI Number

3009537385

📍

Location

New Delhi, Delhi

🇮🇳

Country

INDIA
🏢

Address

18 Cottage, , New Delhi, Delhi, India

Moderate Risk

FDA Import Risk Assessment

47.2
LowModerateHighCritical

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

Statistics

9
Total Refusals
9
Unique Violations
8/14/2012
Latest Refusal
6/22/2012
Earliest Refusal

Score Breakdown

Violation Severity
67.6×40%
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

4824×

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.

164×

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.

1183×

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).

2493×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

753×

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).

2561×

INCONSPICU

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)).

23001×

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.

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.

91×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
8/14/2012
54IGT02PSYLLIUM (FIBER)
2300DIETARYLBL
256INCONSPICU
482NUTRIT LBL
San Francisco District Office (SAN-DO)
8/14/2012
28BGT99SPICES, GROUND, CRACKED, ETC., N.E.C.
249FILTHY
482NUTRIT LBL
San Francisco District Office (SAN-DO)
8/14/2012
28BGT49TURMERIC, GROUND, CRACKED (SPICE)
249FILTHY
482NUTRIT LBL
San Francisco District Office (SAN-DO)
8/14/2012
26CHT11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING
238UNSAFE ADD
482NUTRIT LBL
San Francisco District Office (SAN-DO)
8/14/2012
66VLY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
San Francisco District Office (SAN-DO)
8/14/2012
66VLY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
San Francisco District Office (SAN-DO)
8/14/2012
66VLY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
San Francisco District Office (SAN-DO)
8/14/2012
63RBY06STANNOUS FLUORIDE (DENTAL CARIES PROPHYLACTIC)
16DIRECTIONS
75UNAPPROVED
San Francisco District Office (SAN-DO)
6/22/2012
28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
249FILTHY
9SALMONELLA
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Kore Koncepts's FDA import refusal history?

Kore Koncepts (FEI: 3009537385) has 9 FDA import refusal record(s) in our database, spanning from 6/22/2012 to 8/14/2012.

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. Kore Koncepts's FEI number is 3009537385.

What types of violations has Kore Koncepts received?

Kore Koncepts 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 Kore Koncepts come from?

All FDA import refusal data for Kore Koncepts 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.