QINGDAO HONGTIAN NONGYEKEJI
⚠️ Moderate Risk
FEI: 3015446202 • Qingdao, Shandong • CHINA
FEI Number
3015446202
Location
Qingdao, Shandong
Country
CHINAAddress
Zhongweiyayuan Building A, Laoshan Qu Haier Road, Qingdao, Shandong, 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
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.
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:
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)).
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.
UNFIT4FOOD
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be unfit for food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/27/2020 | 02GGT08SOYBEAN FLOUR, MEAL, OR POWDER | Division of West Coast Imports (DWCI) | |
| 4/1/2020 | 21GGT05DATES (PIT FRUIT), (PIT FRUIT) | 249FILTHY | Division of Northeast Imports (DNEI) |
| 3/28/2020 | 03PGT04PIES AND PUDDING PREPARED DRY MIX WITH CUSTARD OR CREAM FILLING | 324NO ENGLISH | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is QINGDAO HONGTIAN NONGYEKEJI's FDA import refusal history?
QINGDAO HONGTIAN NONGYEKEJI (FEI: 3015446202) has 3 FDA import refusal record(s) in our database, spanning from 3/28/2020 to 8/27/2020.
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. QINGDAO HONGTIAN NONGYEKEJI's FEI number is 3015446202.
What types of violations has QINGDAO HONGTIAN NONGYEKEJI received?
QINGDAO HONGTIAN NONGYEKEJI has been cited for 5 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 QINGDAO HONGTIAN NONGYEKEJI come from?
All FDA import refusal data for QINGDAO HONGTIAN NONGYEKEJI 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.