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Jiangsu Kanion Pharmaceutical Co., Ltd.

⚠️ Moderate Risk

FEI: 3004325596 • Lianyungang, Jiangsu • CHINA

FEI

FEI Number

3004325596

📍

Location

Lianyungang, Jiangsu

🇨🇳

Country

CHINA
🏢

Address

58 Taishanbeilu, , Lianyungang, Jiangsu, China

Moderate Risk

FDA Import Risk Assessment

27.4
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
4/12/2021
Latest Refusal
1/19/2017
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
7.1×10%
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

2562×

INCONSPICU

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)).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
4/12/2021
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/19/2017
54ECF71YARROW ROOT (HERBAL & BOTANICAL TEAS)
256INCONSPICU
Seattle District Office (SEA-DO)
1/19/2017
54ECF48GINKGO BILOBA (HERBAL & BOTANICAL TEAS)
256INCONSPICU
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Jiangsu Kanion Pharmaceutical Co., Ltd.'s FDA import refusal history?

Jiangsu Kanion Pharmaceutical Co., Ltd. (FEI: 3004325596) has 3 FDA import refusal record(s) in our database, spanning from 1/19/2017 to 4/12/2021.

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. Jiangsu Kanion Pharmaceutical Co., Ltd.'s FEI number is 3004325596.

What types of violations has Jiangsu Kanion Pharmaceutical Co., Ltd. received?

Jiangsu Kanion Pharmaceutical Co., Ltd. has been cited for 2 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 Jiangsu Kanion Pharmaceutical Co., Ltd. come from?

All FDA import refusal data for Jiangsu Kanion Pharmaceutical Co., Ltd. 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.