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Guang Zhou Jian Hua

⚠️ Moderate Risk

FEI: 3004044697 • Guang Zhou • CHINA

FEI

FEI Number

3004044697

📍

Location

Guang Zhou

🇨🇳

Country

CHINA
🏢

Address

28 Yuan Yang Xiang, , Guang Zhou, , China

Moderate Risk

FDA Import Risk Assessment

31.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
6
Unique Violations
8/18/2009
Latest Refusal
6/23/2006
Earliest Refusal

Score Breakdown

Violation Severity
58.6×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
9.5×10%
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

2602×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

22001×

DIET INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be for use as an ingredient in a dietary supplement and appears to be or may be otherwise unfit for food.

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

24601×

UNSFDIETLB

The article appears to be a dietary supplement or contain a dietary ingredient that presents a significant or unreasonable risk of illness or injury under the conditions of use set out in the labeling or, if none are set out in the labeling, under customary conditions of use.

3241×

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)).

4881×

HEALTH C

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 bears an unauthorized nutrient content/health claim.

Refusal History

DateProductViolationsDivision
8/18/2009
54YCH10ROYAL JELLY (VIT/MIN/PROTEIN/UNCONVENTIONAL DIETARY SPEC FOR HUMAN/ANIMAL, N.E.C.)
324NO ENGLISH
New Orleans District Office (NOL-DO)
7/31/2006
54FCB99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2200DIET INGRE
223FALSE
260FALSE
Los Angeles District Office (LOS-DO)
6/23/2006
54FCB99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2460UNSFDIETLB
260FALSE
488HEALTH C
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Guang Zhou Jian Hua's FDA import refusal history?

Guang Zhou Jian Hua (FEI: 3004044697) has 3 FDA import refusal record(s) in our database, spanning from 6/23/2006 to 8/18/2009.

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. Guang Zhou Jian Hua's FEI number is 3004044697.

What types of violations has Guang Zhou Jian Hua received?

Guang Zhou Jian Hua 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 Guang Zhou Jian Hua come from?

All FDA import refusal data for Guang Zhou Jian Hua 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.