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Tianjin Foodstuffs Imp & Exp Corp

⚠️ High Risk

FEI: 1000544035 • Tianjin • CHINA

FEI

FEI Number

1000544035

📍

Location

Tianjin

🇨🇳

Country

CHINA
🏢

Address

140 Chi Feng Rd, , Tianjin, , China

High Risk

FDA Import Risk Assessment

54.2
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

20
Total Refusals
8
Unique Violations
9/5/2007
Latest Refusal
11/19/2003
Earliest Refusal

Score Breakdown

Violation Severity
85.7×40%
Refusal Volume
49.0×30%
Recency
0.0×20%
Frequency
52.7×10%
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

2497×

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.

96×

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.

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.

621×

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).

831×

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.

551×

OMITTED

The article is subject to refusal of admission pursuant Section 801(a)(3) of the FD&C Act in that it appears that a valuable constituent of the article has been in whole or in part omitted or abstracted from the article.

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.

2451×

EXCESS SUL

The article appears to contain excessive sulfites, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
9/5/2007
21HGH05DATES, DRIED OR PASTE
249FILTHY
New York District Office (NYK-DO)
3/5/2007
37BCT30BEAN CURD CUBES, FERMENTED (E.G., SALTED) IN OIL/SAUCE/ WINE, ETC. (MULT FOOD SPEC/SIDE DISH/DESSERT
249FILTHY
New York District Office (NYK-DO)
8/18/2006
37BCT30BEAN CURD CUBES, FERMENTED (E.G., SALTED) IN OIL/SAUCE/ WINE, ETC. (MULT FOOD SPEC/SIDE DISH/DESSERT
249FILTHY
New York District Office (NYK-DO)
4/3/2006
25LGH12SWEET POTATO, DRIED OR PASTE
245EXCESS SUL
Chicago District Office (CHI-DO)
3/22/2006
25QGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C.
249FILTHY
Seattle District Office (SEA-DO)
3/22/2006
25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
249FILTHY
Seattle District Office (SEA-DO)
3/2/2005
24BGT07KIDNEY BEAN, DRIED OR PASTE
9SALMONELLA
Los Angeles District Office (LOS-DO)
3/2/2005
24UGH38FERN, BRACKEN, DRIED OR PASTE
9SALMONELLA
Los Angeles District Office (LOS-DO)
3/2/2005
24UGH38FERN, BRACKEN, DRIED OR PASTE
9SALMONELLA
Los Angeles District Office (LOS-DO)
3/2/2005
24UGH99LEAF & STEM VEGETABLES, DRIED OR PASTE, N.E.C.
9SALMONELLA
Los Angeles District Office (LOS-DO)
12/16/2004
24UGH99LEAF & STEM VEGETABLES, DRIED OR PASTE, N.E.C.
9SALMONELLA
Los Angeles District Office (LOS-DO)
12/16/2004
24UGH99LEAF & STEM VEGETABLES, DRIED OR PASTE, N.E.C.
9SALMONELLA
Los Angeles District Office (LOS-DO)
9/14/2004
31PFT99TEA SUBSTITUTES, N.E.C.
260FALSE
Los Angeles District Office (LOS-DO)
9/14/2004
31PFT99TEA SUBSTITUTES, N.E.C.
260FALSE
Los Angeles District Office (LOS-DO)
9/14/2004
31PFT99TEA SUBSTITUTES, N.E.C.
260FALSE
Los Angeles District Office (LOS-DO)
2/4/2004
25PGH01MUSHROOM, COMMON (AGARICUS BISPORUS), WHOLE (BUTTON) (FUNGI)
249FILTHY
New York District Office (NYK-DO)
1/30/2004
27YGT99CONDIMENTS, N.E.C.
328USUAL NAME
New York District Office (NYK-DO)
1/30/2004
27YCT99CONDIMENTS, N.E.C.
55OMITTED
New York District Office (NYK-DO)
1/18/2004
25RGH01MUSHROOM, COMMON (AGARICUS BISPORUS), BROKEN OR KIBBLED
249FILTHY
New York District Office (NYK-DO)
11/19/2003
25EEI99MIXED VEGETABLES, N.E.C.
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Tianjin Foodstuffs Imp & Exp Corp's FDA import refusal history?

Tianjin Foodstuffs Imp & Exp Corp (FEI: 1000544035) has 20 FDA import refusal record(s) in our database, spanning from 11/19/2003 to 9/5/2007.

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. Tianjin Foodstuffs Imp & Exp Corp's FEI number is 1000544035.

What types of violations has Tianjin Foodstuffs Imp & Exp Corp received?

Tianjin Foodstuffs Imp & Exp 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 Tianjin Foodstuffs Imp & Exp Corp come from?

All FDA import refusal data for Tianjin Foodstuffs Imp & Exp 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.