ImportRefusal LogoImportRefusal

St Vincent Electronics

⚠️ Moderate Risk

FEI: 3004173971 • Campden Park, Leeward • SAINT VINCENT AND THE GRENADINES

FEI

FEI Number

3004173971

📍

Location

Campden Park, Leeward

🏢

Address

Campden Park Industrial Estate, , Campden Park, Leeward, Saint Vincent and the Grenadines

Moderate Risk

FDA Import Risk Assessment

36.1
LowModerateHighCritical

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

Statistics

10
Total Refusals
2
Unique Violations
10/3/2008
Latest Refusal
8/20/2007
Earliest Refusal

Score Breakdown

Violation Severity
39.0×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
89.0×10%
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

4739×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

3241×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

Refusal History

DateProductViolationsDivision
10/3/2008
30YYY99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C.
473LABELING
New York District Office (NYK-DO)
10/3/2008
30YYY99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C.
473LABELING
New York District Office (NYK-DO)
10/3/2008
37JCY99SAUCES, N.E.C.
473LABELING
New York District Office (NYK-DO)
10/3/2008
25LGT16CASSAVA, DRIED OR PASTE
473LABELING
New York District Office (NYK-DO)
10/3/2008
37JCY99SAUCES, N.E.C.
473LABELING
New York District Office (NYK-DO)
10/3/2008
37JCY99SAUCES, N.E.C.
473LABELING
New York District Office (NYK-DO)
10/3/2008
37JCY99SAUCES, N.E.C.
473LABELING
New York District Office (NYK-DO)
10/3/2008
29CCY99NONALCOHOLIC BEVERAGES, N.E.C.
473LABELING
New York District Office (NYK-DO)
10/3/2008
29BYY60SODA WATER, CARBONATED
473LABELING
New York District Office (NYK-DO)
8/20/2007
16AGH35SHARK
324NO ENGLISH
New York District Office (NYK-DO)

Frequently Asked Questions

What is St Vincent Electronics's FDA import refusal history?

St Vincent Electronics (FEI: 3004173971) has 10 FDA import refusal record(s) in our database, spanning from 8/20/2007 to 10/3/2008.

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. St Vincent Electronics's FEI number is 3004173971.

What types of violations has St Vincent Electronics received?

St Vincent Electronics 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 St Vincent Electronics come from?

All FDA import refusal data for St Vincent Electronics 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.