ZHONGSHAN CITY WEST AREA DE FENG COMPANY
⚠️ Moderate Risk
FEI: 3010884253 • Zhongshan, Guangdong • CHINA
FEI Number
3010884253
Location
Zhongshan, Guangdong
Country
CHINAAddress
Shalang, , Zhongshan, Guangdong, China
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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).
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
SACCHARLBL
The article appears to contain Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient.
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/19/2017 | 21TGT07PINEAPPLE, DRIED OR PASTE | Division of West Coast Imports (DWCI) | |
| 10/19/2017 | 21TGT07PINEAPPLE, DRIED OR PASTE | Division of West Coast Imports (DWCI) | |
| 10/19/2017 | 21HGT13PEACH, DRIED OR PASTE | Division of West Coast Imports (DWCI) | |
| 10/19/2017 | 21HGT13PEACH, DRIED OR PASTE | Division of West Coast Imports (DWCI) | |
| 10/19/2017 | 21HGT13PEACH, DRIED OR PASTE | Division of West Coast Imports (DWCI) | |
| 10/19/2017 | 21HGT13PEACH, DRIED OR PASTE | Division of West Coast Imports (DWCI) | |
| 10/19/2017 | 21TGT12PASSION FRUIT, DRIED OR PASTE | Division of West Coast Imports (DWCI) | |
| 3/28/2017 | 20BBT24WOLFBERRY (CHINESE OR SOUTHEAST ASIAN BERRY OF THE CHINESE MATRIMONY VINE, W/SLIGHT LICORICE FLAVOR) | Division of West Coast Imports (DWCI) | |
| 1/13/2015 | 25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C. | 249FILTHY | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is ZHONGSHAN CITY WEST AREA DE FENG COMPANY's FDA import refusal history?
ZHONGSHAN CITY WEST AREA DE FENG COMPANY (FEI: 3010884253) has 9 FDA import refusal record(s) in our database, spanning from 1/13/2015 to 10/19/2017.
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. ZHONGSHAN CITY WEST AREA DE FENG COMPANY's FEI number is 3010884253.
What types of violations has ZHONGSHAN CITY WEST AREA DE FENG COMPANY received?
ZHONGSHAN CITY WEST AREA DE FENG COMPANY has been cited for 6 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 ZHONGSHAN CITY WEST AREA DE FENG COMPANY come from?
All FDA import refusal data for ZHONGSHAN CITY WEST AREA DE FENG COMPANY 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.