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JIANGMEN JIANGFAN MARINEPRODUCTS FACTORY

⚠️ Moderate Risk

FEI: 3004657181 • Jiangmen, Guangdong • CHINA

FEI

FEI Number

3004657181

📍

Location

Jiangmen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

70 Jiang Hui Road, Jiangmen City, Jiangmen, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

38.2
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
4/15/2013
Latest Refusal
11/25/2003
Earliest Refusal

Score Breakdown

Violation Severity
72.5×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
5.3×10%
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

833×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

2182×

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.

622×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

2491×

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.

Refusal History

DateProductViolationsDivision
4/15/2013
16YFH07FISH MAW, FISHERY PRODUCTS, N.E.C.
249FILTHY
Division of West Coast Imports (DWCI)
3/25/2004
16MGE08JELLYFISH, OTHER AQUATIC SPECIES
62NEEDS FCE
Los Angeles District Office (LOS-DO)
3/2/2004
24UGH99LEAF & STEM VEGETABLES, DRIED OR PASTE, N.E.C.
218LIST INGRE
83NO PROCESS
Los Angeles District Office (LOS-DO)
3/2/2004
24UGE29SEAWEED, DRIED OR PASTE
218LIST INGRE
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
11/25/2003
16MGT08JELLYFISH, OTHER AQUATIC SPECIES
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is JIANGMEN JIANGFAN MARINEPRODUCTS FACTORY's FDA import refusal history?

JIANGMEN JIANGFAN MARINEPRODUCTS FACTORY (FEI: 3004657181) has 5 FDA import refusal record(s) in our database, spanning from 11/25/2003 to 4/15/2013.

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. JIANGMEN JIANGFAN MARINEPRODUCTS FACTORY's FEI number is 3004657181.

What types of violations has JIANGMEN JIANGFAN MARINEPRODUCTS FACTORY received?

JIANGMEN JIANGFAN MARINEPRODUCTS FACTORY has been cited for 4 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 JIANGMEN JIANGFAN MARINEPRODUCTS FACTORY come from?

All FDA import refusal data for JIANGMEN JIANGFAN MARINEPRODUCTS FACTORY 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.