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VIVIAN COMPANY LIMITED

⚠️ Moderate Risk

FEI: 3005384780 • Long Ho District, Vinh Long • VIETNAM

FEI

FEI Number

3005384780

📍

Location

Long Ho District, Vinh Long

🇻🇳

Country

VIETNAM
🏢

Address

118A/09, Thanh My 1 Hamlet, Thanh Duc Village, Long Ho District, Vinh Long, Vietnam

Moderate Risk

FDA Import Risk Assessment

43.5
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
2/22/2017
Latest Refusal
7/3/2013
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
8.2×10%
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

37213×

PESTICIDE2

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

Refusal History

DateProductViolationsDivision
2/22/2017
25PEE03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI)
3721PESTICIDE2
Los Angeles District Office (LOS-DO)
8/14/2013
25PEE03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI)
3721PESTICIDE2
New York District Office (NYK-DO)
7/3/2013
25PEE03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI)
3721PESTICIDE2
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is VIVIAN COMPANY LIMITED's FDA import refusal history?

VIVIAN COMPANY LIMITED (FEI: 3005384780) has 3 FDA import refusal record(s) in our database, spanning from 7/3/2013 to 2/22/2017.

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. VIVIAN COMPANY LIMITED's FEI number is 3005384780.

What types of violations has VIVIAN COMPANY LIMITED received?

VIVIAN COMPANY LIMITED 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 VIVIAN COMPANY LIMITED come from?

All FDA import refusal data for VIVIAN COMPANY LIMITED 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.