GUANGZHOU QINGXINTANG ZHIYAO COLTD
⚠️ Moderate Risk
FEI: 3014127563 • Guangzhou, Guangdong • CHINA
FEI Number
3014127563
Location
Guangzhou, Guangdong
Country
CHINAAddress
16 Gejifang Zianbin, , Guangzhou, 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
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.
Refusal History
Frequently Asked Questions
What is GUANGZHOU QINGXINTANG ZHIYAO COLTD's FDA import refusal history?
GUANGZHOU QINGXINTANG ZHIYAO COLTD (FEI: 3014127563) has 3 FDA import refusal record(s) in our database, spanning from 11/10/2020 to 12/28/2020.
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. GUANGZHOU QINGXINTANG ZHIYAO COLTD's FEI number is 3014127563.
What types of violations has GUANGZHOU QINGXINTANG ZHIYAO COLTD received?
GUANGZHOU QINGXINTANG ZHIYAO COLTD has been cited for 1 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 QINGXINTANG ZHIYAO COLTD come from?
All FDA import refusal data for GUANGZHOU QINGXINTANG ZHIYAO COLTD 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.