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Nanjing Changli Sugar Product Co., Ltd

✅ Low Risk

FEI: 3006800311 • Nanjing, Jiangsu • CHINA

FEI

FEI Number

3006800311

📍

Location

Nanjing, Jiangsu

🇨🇳

Country

CHINA
🏢

Address

288 Zhenzhu North Rd, Yongyangzhen Lishuixian, Nanjing, Jiangsu, China

Low Risk

FDA Import Risk Assessment

21.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

2
Total Refusals
4
Unique Violations
10/29/2008
Latest Refusal
10/29/2008
Earliest Refusal

Score Breakdown

Violation Severity
35.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

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.

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.

3212×

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.

3282×

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.

Refusal History

DateProductViolationsDivision
10/29/2008
36BEE02GLUCOSE AND CORN SYRUP
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Southwest Import District Office (SWI-DO)
10/29/2008
36BEE10BLENDED SYRUPS, PANCAKE AND WAFFLE SYRUP
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Nanjing Changli Sugar Product Co., Ltd's FDA import refusal history?

Nanjing Changli Sugar Product Co., Ltd (FEI: 3006800311) has 2 FDA import refusal record(s) in our database, spanning from 10/29/2008 to 10/29/2008.

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. Nanjing Changli Sugar Product Co., Ltd's FEI number is 3006800311.

What types of violations has Nanjing Changli Sugar Product Co., Ltd received?

Nanjing Changli Sugar Product Co., Ltd 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 Nanjing Changli Sugar Product Co., Ltd come from?

All FDA import refusal data for Nanjing Changli Sugar Product 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.