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DAVE & BECK FOODS

⚠️ Moderate Risk

FEI: 3010919958 • Trichy, Tamil Nadu • INDIA

FEI

FEI Number

3010919958

📍

Location

Trichy, Tamil Nadu

🇮🇳

Country

INDIA
🏢

Address

Panamangalam Old Road, Kuthur Post, 4/157; A Kudi Street, Trichy, Tamil Nadu, India

Moderate Risk

FDA Import Risk Assessment

37.1
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
8/10/2023
Latest Refusal
10/4/2017
Earliest Refusal

Score Breakdown

Violation Severity
53.3×40%
Refusal Volume
25.9×30%
Recency
36.7×20%
Frequency
6.8×10%
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

3283×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

4823×

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.

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.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

91×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
8/10/2023
28AGH54PEPPER,BLACK, WHOLE (SPICE)
249FILTHY
9SALMONELLA
Division of Southeast Imports (DSEI)
10/4/2017
02DFO99RICE, PROCESSED (PACKAGED) N.E.C.
328USUAL NAME
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
10/4/2017
02DFO99RICE, PROCESSED (PACKAGED) N.E.C.
328USUAL NAME
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
10/4/2017
02DFO99RICE, PROCESSED (PACKAGED) N.E.C.
218LIST INGRE
328USUAL NAME
482NUTRIT LBL
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is DAVE & BECK FOODS's FDA import refusal history?

DAVE & BECK FOODS (FEI: 3010919958) has 4 FDA import refusal record(s) in our database, spanning from 10/4/2017 to 8/10/2023.

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. DAVE & BECK FOODS's FEI number is 3010919958.

What types of violations has DAVE & BECK FOODS received?

DAVE & BECK FOODS has been cited for 5 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 DAVE & BECK FOODS come from?

All FDA import refusal data for DAVE & BECK FOODS 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.