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Shantou Ruiyuan Industry Co., Ltd.

⚠️ Moderate Risk

FEI: 3004067667 • Shantou, Guangdong • CHINA

FEI

FEI Number

3004067667

📍

Location

Shantou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

No. 7 Shengye Rd., Shengping Industry District, Shantou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

48.5
LowModerateHighCritical

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

Statistics

17
Total Refusals
7
Unique Violations
12/11/2012
Latest Refusal
7/27/2004
Earliest Refusal

Score Breakdown

Violation Severity
81.3×40%
Refusal Volume
46.5×30%
Recency
0.0×20%
Frequency
20.3×10%
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

98×

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.

28605×

VETDRUGRES

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of Section 512. Product contains

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.

2603×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

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.

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.

33201×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

Refusal History

DateProductViolationsDivision
12/11/2012
16MGD01FROG LEGS, OTHER AQUATIC SPECIES
2860VETDRUGRES
Los Angeles District Office (LOS-DO)
1/29/2010
16XGT42FROGS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
Chicago District Office (CHI-DO)
1/19/2010
16XGT42FROGS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
New England District Office (NWE-DO)
1/2/2010
16XGT42FROGS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
New England District Office (NWE-DO)
12/10/2009
16XGT42FROGS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
New England District Office (NWE-DO)
7/22/2009
16WGT99MIXED FISHERY/SEAFOOD PRODUCTS, N.E.C.
218LIST INGRE
249FILTHY
3320TRANSFAT
Seattle District Office (SEA-DO)
2/17/2009
16XVT42FROGS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
9SALMONELLA
New England District Office (NWE-DO)
1/14/2008
16MGT01FROG LEGS, OTHER AQUATIC SPECIES
9SALMONELLA
Atlanta District Office (ATL-DO)
12/28/2007
16XGT42FROGS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
320LACKS FIRM
9SALMONELLA
New England District Office (NWE-DO)
11/21/2006
16MGD03SQUID, OTHER AQUATIC SPECIES
249FILTHY
260FALSE
Seattle District Office (SEA-DO)
11/21/2006
16MGD03SQUID, OTHER AQUATIC SPECIES
249FILTHY
260FALSE
Seattle District Office (SEA-DO)
11/21/2006
16MGD03SQUID, OTHER AQUATIC SPECIES
249FILTHY
260FALSE
Seattle District Office (SEA-DO)
10/12/2005
16MGT03SQUID, OTHER AQUATIC SPECIES
9SALMONELLA
New England District Office (NWE-DO)
7/27/2004
16MHT01FROG LEGS, OTHER AQUATIC SPECIES
9SALMONELLA
New England District Office (NWE-DO)
7/27/2004
16MHT01FROG LEGS, OTHER AQUATIC SPECIES
9SALMONELLA
New England District Office (NWE-DO)
7/27/2004
16MHT01FROG LEGS, OTHER AQUATIC SPECIES
9SALMONELLA
New England District Office (NWE-DO)
7/27/2004
16MHT01FROG LEGS, OTHER AQUATIC SPECIES
9SALMONELLA
New England District Office (NWE-DO)

Frequently Asked Questions

What is Shantou Ruiyuan Industry Co., Ltd.'s FDA import refusal history?

Shantou Ruiyuan Industry Co., Ltd. (FEI: 3004067667) has 17 FDA import refusal record(s) in our database, spanning from 7/27/2004 to 12/11/2012.

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. Shantou Ruiyuan Industry Co., Ltd.'s FEI number is 3004067667.

What types of violations has Shantou Ruiyuan Industry Co., Ltd. received?

Shantou Ruiyuan Industry Co., Ltd. has been cited for 7 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 Shantou Ruiyuan Industry Co., Ltd. come from?

All FDA import refusal data for Shantou Ruiyuan Industry 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.