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Takezawa Seicha

⚠️ Moderate Risk

FEI: 3004337657 • Shizuoka, Shizuoka • JAPAN

FEI

FEI Number

3004337657

📍

Location

Shizuoka, Shizuoka

🇯🇵

Country

JAPAN
🏢

Address

61-2 Kitaban-Cho, Aoi; Kitaban-Cho; Aoi, Shizuoka, Shizuoka, Japan

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
12/12/2018
Latest Refusal
12/12/2018
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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

4821×

NUTRIT LBL

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 fails to bear the required nutrition information.

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
12/12/2018
54EBR99HERBALS & BOTANICAL TEAS, N.E.C.
482NUTRIT LBL
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Takezawa Seicha's FDA import refusal history?

Takezawa Seicha (FEI: 3004337657) has 1 FDA import refusal record(s) in our database, spanning from 12/12/2018 to 12/12/2018.

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. Takezawa Seicha's FEI number is 3004337657.

What types of violations has Takezawa Seicha received?

Takezawa Seicha 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 Takezawa Seicha come from?

All FDA import refusal data for Takezawa Seicha 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.