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Xiamen Wisdomaromatic Co., Ltd.

⚠️ Moderate Risk

FEI: 3012189061 • Shamen, Fujian • CHINA

FEI

FEI Number

3012189061

📍

Location

Shamen, Fujian

🇨🇳

Country

CHINA
🏢

Address

No. F 4, N 3P 5 Factory Huangjin I; Tongan, Shamen, Fujian, China

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
6/20/2016
Latest Refusal
6/20/2016
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

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
6/20/2016
54YDZ99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Xiamen Wisdomaromatic Co., Ltd.'s FDA import refusal history?

Xiamen Wisdomaromatic Co., Ltd. (FEI: 3012189061) has 1 FDA import refusal record(s) in our database, spanning from 6/20/2016 to 6/20/2016.

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. Xiamen Wisdomaromatic Co., Ltd.'s FEI number is 3012189061.

What types of violations has Xiamen Wisdomaromatic Co., Ltd. received?

Xiamen Wisdomaromatic Co., Ltd. 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 Xiamen Wisdomaromatic Co., Ltd. come from?

All FDA import refusal data for Xiamen Wisdomaromatic 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.