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ANGUOSHI TIANXIAKANG PHARMACEUTICAL CO., LTD

⚠️ Moderate Risk

FEI: 3008775043 • Anguo, Hebei • CHINA

FEI

FEI Number

3008775043

📍

Location

Anguo, Hebei

🇨🇳

Country

CHINA
🏢

Address

Qizhou Industrial City, , Anguo, Hebei, China

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
10/13/2016
Latest Refusal
10/13/2016
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

2511×

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:

Refusal History

DateProductViolationsDivision
10/13/2016
54FBT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
251POISONOUS
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is ANGUOSHI TIANXIAKANG PHARMACEUTICAL CO., LTD's FDA import refusal history?

ANGUOSHI TIANXIAKANG PHARMACEUTICAL CO., LTD (FEI: 3008775043) has 1 FDA import refusal record(s) in our database, spanning from 10/13/2016 to 10/13/2016.

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. ANGUOSHI TIANXIAKANG PHARMACEUTICAL CO., LTD's FEI number is 3008775043.

What types of violations has ANGUOSHI TIANXIAKANG PHARMACEUTICAL CO., LTD received?

ANGUOSHI TIANXIAKANG PHARMACEUTICAL 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 ANGUOSHI TIANXIAKANG PHARMACEUTICAL CO., LTD come from?

All FDA import refusal data for ANGUOSHI TIANXIAKANG 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.