ImportRefusal LogoImportRefusal

XIAMEN TANSHI TECHNOLOGY CO.,LTD

⚠️ High Risk

FEI: 3007136139 • Xiamen, Fujian • CHINA

FEI

FEI Number

3007136139

📍

Location

Xiamen, Fujian

🇨🇳

Country

CHINA
🏢

Address

Room 16, No. 9 Siming North Rd; District,Xiamen, Xiamen, Fujian, China

High Risk

FDA Import Risk Assessment

58.2
LowModerateHighCritical

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

Statistics

17
Total Refusals
10
Unique Violations
8/26/2009
Latest Refusal
1/26/2009
Earliest Refusal

Score Breakdown

Violation Severity
85.7×40%
Refusal Volume
46.5×30%
Recency
0.0×20%
Frequency
100.0×10%
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

2496×

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.

34215×

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.

34223×

UNFIT4FOOD

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be unfit for food.

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.

2512×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

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.

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.

3241×

NO ENGLISH

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)).

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).

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

Refusal History

DateProductViolationsDivision
8/26/2009
09YEE99FLUID/DRY MILK PRODUCTS NOT ELSEWHERE MENTIONED, N.E.C.
3421MELAMINE
New York District Office (NYK-DO)
8/26/2009
33SGE99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
482NUTRIT LBL
New York District Office (NYK-DO)
8/26/2009
16EGE06CONCH,CONCHMEAT
482NUTRIT LBL
New York District Office (NYK-DO)
8/26/2009
31KGE99TEA, N.E.C.
324NO ENGLISH
New York District Office (NYK-DO)
8/26/2009
04YGE02RICE VERMICELLI
249FILTHY
New York District Office (NYK-DO)
8/26/2009
28YGE99SPICES, FLAVORS AND SALT NOT MENTIONED ELSEWHERE, N.E.C.
218LIST INGRE
New York District Office (NYK-DO)
8/26/2009
21GGE05DATES (PIT FRUIT), (PIT FRUIT)
11UNSAFE COL
New York District Office (NYK-DO)
7/10/2009
37BGE28BEAN CURD, DRIED (STICKS, SHEETS), (MULTIPLE FOOD SPECIALTIES, SIDE DISHES AND DESSERTS
249FILTHY
New York District Office (NYK-DO)
7/9/2009
25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
249FILTHY
New York District Office (NYK-DO)
7/9/2009
25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
249FILTHY
New York District Office (NYK-DO)
5/8/2009
29AGT99NONCARBONATED SOFT DRINK, N.E.C.
3421MELAMINE
New York District Office (NYK-DO)
5/8/2009
04YGT02RICE VERMICELLI
249FILTHY
New York District Office (NYK-DO)
4/8/2009
03MGT99COOKIE,BISCUIT,WAFER DOUGH, N.E.C.
3421MELAMINE
3422UNFIT4FOOD
New York District Office (NYK-DO)
4/3/2009
29AGT99NONCARBONATED SOFT DRINK, N.E.C.
251POISONOUS
3421MELAMINE
3422UNFIT4FOOD
New York District Office (NYK-DO)
4/3/2009
03MGT99COOKIE,BISCUIT,WAFER DOUGH, N.E.C.
251POISONOUS
3421MELAMINE
3422UNFIT4FOOD
New York District Office (NYK-DO)
1/30/2009
29AGE99NONCARBONATED SOFT DRINK, N.E.C.
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
1/26/2009
04YGT02RICE VERMICELLI
249FILTHY
New York District Office (NYK-DO)

Frequently Asked Questions

What is XIAMEN TANSHI TECHNOLOGY CO.,LTD's FDA import refusal history?

XIAMEN TANSHI TECHNOLOGY CO.,LTD (FEI: 3007136139) has 17 FDA import refusal record(s) in our database, spanning from 1/26/2009 to 8/26/2009.

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. XIAMEN TANSHI TECHNOLOGY CO.,LTD's FEI number is 3007136139.

What types of violations has XIAMEN TANSHI TECHNOLOGY CO.,LTD received?

XIAMEN TANSHI TECHNOLOGY CO.,LTD has been cited for 10 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 XIAMEN TANSHI TECHNOLOGY CO.,LTD come from?

All FDA import refusal data for XIAMEN TANSHI TECHNOLOGY 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.