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Hubei Best Source Trading Inc.

⚠️ Moderate Risk

FEI: 3012056879 • Hubei • CHINA

FEI

FEI Number

3012056879

📍

Location

Hubei

🇨🇳

Country

CHINA
🏢

Address

No. 58 Yiling Ave, Suite 4-1119 Yichang, , Hubei, , China

Moderate Risk

FDA Import Risk Assessment

33.6
LowModerateHighCritical

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

Statistics

6
Total Refusals
8
Unique Violations
12/16/2019
Latest Refusal
12/16/2019
Earliest Refusal

Score Breakdown

Violation Severity
45.5×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
60.0×10%
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

3206×

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.

2185×

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.

2565×

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)).

3215×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

4733×

LABELING

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

33003×

ALLERGEN

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

34213×

MELAMINE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to bear or contain a food additive, namely melamine and/or a melamine analog, that is unsafe within the meaning of section 409.

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

Refusal History

DateProductViolationsDivision
12/16/2019
23AGT12WALNUTS, BLACK, ENGLISH OR PERSIAN, IN SHELL
256INCONSPICU
320LACKS FIRM
328USUAL NAME
3300ALLERGEN
473LABELING
Division of West Coast Imports (DWCI)
12/16/2019
23HGT99MIXED NUTS, SHELLED, N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
3300ALLERGEN
473LABELING
Division of West Coast Imports (DWCI)
12/16/2019
02FGT08GLUTEN, WHEAT
218LIST INGRE
256INCONSPICU
320LACKS FIRM
321LACKS N/C
3421MELAMINE
Division of West Coast Imports (DWCI)
12/16/2019
02FGT08GLUTEN, WHEAT
218LIST INGRE
256INCONSPICU
320LACKS FIRM
321LACKS N/C
3421MELAMINE
Division of West Coast Imports (DWCI)
12/16/2019
02FGT08GLUTEN, WHEAT
218LIST INGRE
256INCONSPICU
320LACKS FIRM
321LACKS N/C
3421MELAMINE
Division of West Coast Imports (DWCI)
12/16/2019
07QGT08SEAWEED SNACKS (FLAVORED OR UNFLAVORED), VEGETABLE SNACKS (OTHER THAN PULSES) BAKED
218LIST INGRE
256INCONSPICU
320LACKS FIRM
321LACKS N/C
3300ALLERGEN
473LABELING
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Hubei Best Source Trading Inc.'s FDA import refusal history?

Hubei Best Source Trading Inc. (FEI: 3012056879) has 6 FDA import refusal record(s) in our database, spanning from 12/16/2019 to 12/16/2019.

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. Hubei Best Source Trading Inc.'s FEI number is 3012056879.

What types of violations has Hubei Best Source Trading Inc. received?

Hubei Best Source Trading Inc. has been cited for 8 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 Hubei Best Source Trading Inc. come from?

All FDA import refusal data for Hubei Best Source Trading Inc. 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.