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GUANGZHOU RUNMEI SHI PING YINLIAO

⚠️ Moderate Risk

FEI: 3015446222 • Guangzhou, Guangdong • CHINA

FEI

FEI Number

3015446222

📍

Location

Guangzhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Renhezhen Daxiangcun Suite, 8 Tonggui Road, Guangzhou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

48.7
LowModerateHighCritical

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

Statistics

4
Total Refusals
7
Unique Violations
10/29/2025
Latest Refusal
9/26/2019
Earliest Refusal

Score Breakdown

Violation Severity
52.9×40%
Refusal Volume
25.9×30%
Recency
95.5×20%
Frequency
6.6×10%
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

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.

26401×

CYCLAMATE

The article appears to bear or contain cyclamate, an unsafe food additive within the meaning of Section 409

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

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.

3211×

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.

34211×

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.

4821×

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.

Refusal History

DateProductViolationsDivision
10/29/2025
20AGT19HAW
274COLOR LBLG
Division of Northern Border Imports (DNBI)
10/5/2023
36BGT99SYRUPS AND MOLASSES, N.E.C.
2640CYCLAMATE
Division of Northern Border Imports (DNBI)
8/31/2023
20KGT02GRAPEFRUIT, CITRUS FRUIT JUICES OR CONCENTRATES
218LIST INGRE
320LACKS FIRM
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
9/26/2019
34YYY99CHOCOLATE AND COCOA PRODUCTS, N.E.C.
3421MELAMINE
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is GUANGZHOU RUNMEI SHI PING YINLIAO's FDA import refusal history?

GUANGZHOU RUNMEI SHI PING YINLIAO (FEI: 3015446222) has 4 FDA import refusal record(s) in our database, spanning from 9/26/2019 to 10/29/2025.

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. GUANGZHOU RUNMEI SHI PING YINLIAO's FEI number is 3015446222.

What types of violations has GUANGZHOU RUNMEI SHI PING YINLIAO received?

GUANGZHOU RUNMEI SHI PING YINLIAO 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 GUANGZHOU RUNMEI SHI PING YINLIAO come from?

All FDA import refusal data for GUANGZHOU RUNMEI SHI PING YINLIAO 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.