FUJIAN JIWANG RD IMPORT AND EX
⚠️ High Risk
FEI: 3016249923 • Fuzhou City • CHINA
FEI Number
3016249923
Location
Fuzhou City
Country
CHINAAddress
Building 7 F 23, Square East 2nd Ring Rd; Taihe City, Fuzhou City, , China
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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.
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.
INADPRCCTL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate process controls.
UNFIT4FOOD
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be unfit for food.
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:
FSVP VIO
The article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) in that it appears that the importer (as defined in section 805 of the FD&C Act) is in violation of section 805.
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.
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.
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.
POISONORD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a poisonous or deleterious substance which would ordinarily render the article injurious to health. Contains:
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/12/2025 | 24UGY03BAMBOO SHOOTS, DRIED OR PASTE | Division of Northeast Imports (DNEI) | |
| 12/12/2025 | 24UGY03BAMBOO SHOOTS, DRIED OR PASTE | Division of Northeast Imports (DNEI) | |
| 5/4/2023 | 21HGT16CHINESE RED DATE (JUJUBES, ZIZIPHUS JUJUBA), DRIED OR PASTE | 249FILTHY | Division of Northeast Imports (DNEI) |
| 4/6/2022 | 03YGT99OTHER BAKERY PRODUCTS, N.E.C. | 3886FSVP VIO | Division of Northeast Imports (DNEI) |
| 3/30/2022 | 07AGT05POPCORN, POPPED, BAKED | 3886FSVP VIO | Division of Northeast Imports (DNEI) |
| 8/5/2021 | 07SGT99STARCH SNACKS, N.E.C., BAKED | 3421MELAMINE | Division of Northeast Imports (DNEI) |
| 3/12/2021 | 09HFT10YOGURT, ALL TYPE (GREEK, STRAINED, FLAVORED), GRADE A | Division of Northeast Imports (DNEI) | |
| 2/26/2021 | 29AFT70SOFT DRINK, MILK BASED (CHOCOLATE FLAVORED, ETC.), NONCARBONATED | 3421MELAMINE | Division of Northeast Imports (DNEI) |
| 8/6/2020 | 29AET99NONCARBONATED SOFT DRINK, N.E.C. | 3421MELAMINE | Division of Northeast Imports (DNEI) |
| 6/23/2020 | 29AEE99NONCARBONATED SOFT DRINK, N.E.C. | Division of Northeast Imports (DNEI) | |
| 5/6/2020 | 07BGN06POTATO CHIPS,FRIED | Division of Northeast Imports (DNEI) | |
| 5/6/2020 | 02FGT08GLUTEN, WHEAT | 3421MELAMINE | Division of Northeast Imports (DNEI) |
| 4/3/2020 | 41YGT99DIETARY CONVENTIONAL FOODS, N.E.C. | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is FUJIAN JIWANG RD IMPORT AND EX's FDA import refusal history?
FUJIAN JIWANG RD IMPORT AND EX (FEI: 3016249923) has 13 FDA import refusal record(s) in our database, spanning from 4/3/2020 to 12/12/2025.
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. FUJIAN JIWANG RD IMPORT AND EX's FEI number is 3016249923.
What types of violations has FUJIAN JIWANG RD IMPORT AND EX received?
FUJIAN JIWANG RD IMPORT AND EX has been cited for 11 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 FUJIAN JIWANG RD IMPORT AND EX come from?
All FDA import refusal data for FUJIAN JIWANG RD IMPORT AND EX 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.