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VIANCO Joint Venture Enterprise

⚠️ Moderate Risk

FEI: 3004262683 • Ho Chi Minh City, VN-65 • VIETNAM

FEI

FEI Number

3004262683

📍

Location

Ho Chi Minh City, VN-65

🇻🇳

Country

VIETNAM
🏢

Address

451/5 Nguyen Trai Street, Ward 7 District 5, Ho Chi Minh City, VN-65, Vietnam

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
2/15/2011
Latest Refusal
2/15/2011
Earliest Refusal

Score Breakdown

Violation Severity
53.3×40%
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

2181×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2761×

PRESRV LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.

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
2/15/2011
37KCE99PASTES, N.E.C.
218LIST INGRE
276PRESRV LBL
83NO PROCESS
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is VIANCO Joint Venture Enterprise's FDA import refusal history?

VIANCO Joint Venture Enterprise (FEI: 3004262683) has 1 FDA import refusal record(s) in our database, spanning from 2/15/2011 to 2/15/2011.

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. VIANCO Joint Venture Enterprise's FEI number is 3004262683.

What types of violations has VIANCO Joint Venture Enterprise received?

VIANCO Joint Venture Enterprise has been cited for 3 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 VIANCO Joint Venture Enterprise come from?

All FDA import refusal data for VIANCO Joint Venture Enterprise 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.