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New Concept Product Co., Ltd.

⚠️ Moderate Risk

FEI: 3007670906 • Phan Thong, Chon Buri • THAILAND

FEI

FEI Number

3007670906

📍

Location

Phan Thong, Chon Buri

🇹🇭

Country

THAILAND
🏢

Address

700/291 Amata Nakorn Industrial Estate, Moo 1, Bankao, Phan Thong, Chon Buri, Thailand

Moderate Risk

FDA Import Risk Assessment

31.9
LowModerateHighCritical

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

Statistics

7
Total Refusals
10
Unique Violations
4/17/2017
Latest Refusal
9/28/2010
Earliest Refusal

Score Breakdown

Violation Severity
51.9×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
10.7×10%
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

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.

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).

3242×

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)).

4882×

HEALTH C

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 bears an unauthorized nutrient content/health claim.

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.

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.

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.

2181×

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.

2621×

DIETARY

The article purports to be or is represented for special dietary uses and its label does not appear to bear the nutritional information required by regulation.

Refusal History

DateProductViolationsDivision
4/17/2017
31KFT02TEA, GREEN
324NO ENGLISH
Division of West Coast Imports (DWCI)
9/25/2014
31KGT02TEA, GREEN
218LIST INGRE
320LACKS FIRM
324NO ENGLISH
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
10/16/2012
54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Minneapolis District Office (MIN-DO)
10/16/2012
54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Minneapolis District Office (MIN-DO)
3/17/2011
31KFT02TEA, GREEN
262DIETARY
482NUTRIT LBL
488HEALTH C
Los Angeles District Office (LOS-DO)
9/28/2010
54FCT10GARLIC (HERBAL & BOTANICALS, NOT TEAS)
2300DIETARYLBL
482NUTRIT LBL
488HEALTH C
Los Angeles District Office (LOS-DO)
9/28/2010
66VBU99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
335LACKS N/C
75UNAPPROVED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is New Concept Product Co., Ltd.'s FDA import refusal history?

New Concept Product Co., Ltd. (FEI: 3007670906) has 7 FDA import refusal record(s) in our database, spanning from 9/28/2010 to 4/17/2017.

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. New Concept Product Co., Ltd.'s FEI number is 3007670906.

What types of violations has New Concept Product Co., Ltd. received?

New Concept Product Co., 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 New Concept Product Co., Ltd. come from?

All FDA import refusal data for New Concept Product Co., 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.