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K & B Manufacturing

⚠️ Moderate Risk

FEI: 3010242733 • Ahmedabad, Gujarat • INDIA

FEI

FEI Number

3010242733

📍

Location

Ahmedabad, Gujarat

🇮🇳

Country

INDIA
🏢

Address

38 Pamping Station, , Ahmedabad, Gujarat, India

Moderate Risk

FDA Import Risk Assessment

33.6
LowModerateHighCritical

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

Statistics

4
Total Refusals
6
Unique Violations
7/10/2019
Latest Refusal
3/31/2016
Earliest Refusal

Score Breakdown

Violation Severity
61.7×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
12.2×10%
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

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.

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

3201×

LACKS FIRM

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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

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
7/10/2019
07YGT99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C.
274COLOR LBLG
Division of Northeast Imports (DNEI)
5/6/2019
07YGT99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C.
249FILTHY
Division of Northeast Imports (DNEI)
7/28/2017
37JGT99SAUCES, N.E.C.
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
3/31/2016
28JGT99MIXED SPICES AND SEASONING WITH SALT, N.E.C.
218LIST INGRE
320LACKS FIRM
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is K & B Manufacturing's FDA import refusal history?

K & B Manufacturing (FEI: 3010242733) has 4 FDA import refusal record(s) in our database, spanning from 3/31/2016 to 7/10/2019.

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. K & B Manufacturing's FEI number is 3010242733.

What types of violations has K & B Manufacturing received?

K & B Manufacturing has been cited for 6 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 K & B Manufacturing come from?

All FDA import refusal data for K & B Manufacturing 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.