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GUANGDONG DONG FANG IMP & EXP GUANGZHOU CORP.

⚠️ Moderate Risk

FEI: 3004337250 • Guangzhou, Guangdong • CHINA

FEI

FEI Number

3004337250

📍

Location

Guangzhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Xilang Liuxiang Market 2, 12 No. 60 3rd Road Street; Liwan, Guangzhou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

34.7
LowModerateHighCritical

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

Statistics

7
Total Refusals
8
Unique Violations
6/12/2014
Latest Refusal
3/9/2004
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
6.8×10%
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

2494×

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.

3202×

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.

4822×

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.

37211×

PESTICIDE2

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

4731×

LABELING

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

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.

3211×

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.

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.

Refusal History

DateProductViolationsDivision
6/12/2014
25SGH09FUNGUS, BLACK (CLOUD EARS), FUNGI PRODUCTS, N.E.C.
3721PESTICIDE2
San Francisco District Office (SAN-DO)
3/16/2010
54FBT03ANGELICA (HERBAL & BOTANICALS, NOT TEAS)
2300DIETARYLBL
320LACKS FIRM
473LABELING
482NUTRIT LBL
San Francisco District Office (SAN-DO)
3/16/2010
25SGH10FUNGUS, WHITE, FUNGI PRODUCTS, N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
San Francisco District Office (SAN-DO)
6/29/2004
25PGH04MUSHROOM, SHIITAKE , WHOLE (BUTTON) (FUNGI)
249FILTHY
San Francisco District Office (SAN-DO)
6/29/2004
25PGH04MUSHROOM, SHIITAKE , WHOLE (BUTTON) (FUNGI)
249FILTHY
San Francisco District Office (SAN-DO)
6/29/2004
25PGH04MUSHROOM, SHIITAKE , WHOLE (BUTTON) (FUNGI)
249FILTHY
San Francisco District Office (SAN-DO)
3/9/2004
16YGH07FISH MAW, FISHERY PRODUCTS, N.E.C.
249FILTHY
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is GUANGDONG DONG FANG IMP & EXP GUANGZHOU CORP.'s FDA import refusal history?

GUANGDONG DONG FANG IMP & EXP GUANGZHOU CORP. (FEI: 3004337250) has 7 FDA import refusal record(s) in our database, spanning from 3/9/2004 to 6/12/2014.

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. GUANGDONG DONG FANG IMP & EXP GUANGZHOU CORP.'s FEI number is 3004337250.

What types of violations has GUANGDONG DONG FANG IMP & EXP GUANGZHOU CORP. received?

GUANGDONG DONG FANG IMP & EXP GUANGZHOU CORP. 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 GUANGDONG DONG FANG IMP & EXP GUANGZHOU CORP. come from?

All FDA import refusal data for GUANGDONG DONG FANG IMP & EXP GUANGZHOU CORP. 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.