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BIOPAX LTD

⚠️ Moderate Risk

FEI: 3022503028 • Taichung • TAIWAN

FEI

FEI Number

3022503028

📍

Location

Taichung

🇹🇼

Country

TAIWAN
🏢

Address

3f-1 No 75 Sec 2 Meicun, , Taichung, , Taiwan

Moderate Risk

FDA Import Risk Assessment

46.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
1/18/2024
Latest Refusal
1/18/2024
Earliest Refusal

Score Breakdown

Violation Severity
68.0×40%
Refusal Volume
22.3×30%
Recency
45.3×20%
Frequency
30.0×10%
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

23002×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

33001×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

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).

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
1/18/2024
54ACY99VITAMIN, N.E.C.
2300DIETARYLBL
3300ALLERGEN
75UNAPPROVED
Division of Northeast Imports (DNEI)
1/18/2024
54ACY99VITAMIN, N.E.C.
2300DIETARYLBL
Division of Northeast Imports (DNEI)
1/18/2024
54FCY94ASHWAGANDHA (HERBAL & BOTANICALS, NOT TEAS)
83NO PROCESS
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is BIOPAX LTD's FDA import refusal history?

BIOPAX LTD (FEI: 3022503028) has 3 FDA import refusal record(s) in our database, spanning from 1/18/2024 to 1/18/2024.

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. BIOPAX LTD's FEI number is 3022503028.

What types of violations has BIOPAX LTD received?

BIOPAX LTD has been cited for 4 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 BIOPAX LTD come from?

All FDA import refusal data for BIOPAX 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.