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K.K. International

⚠️ Moderate Risk

FEI: 3005213464 • Mumbai, Maharashtra • INDIA

FEI

FEI Number

3005213464

📍

Location

Mumbai, Maharashtra

🇮🇳

Country

INDIA
🏢

Address

X - 13 Shashtri Nagar, Grden View, Mumbai, Maharashtra, India

Moderate Risk

FDA Import Risk Assessment

40.4
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
4/3/2007
Latest Refusal
4/3/2007
Earliest Refusal

Score Breakdown

Violation Severity
71.7×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

2492×

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.

3211×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

4821×

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.

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
4/3/2007
03HGT08BUTTER/BUTTER FLAVORED,PLAIN COOKIES,BISCUITS AND WAFERS
321LACKS N/C
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
4/3/2007
07BGT99FRIED SNACK FOODS, N.E.C.
249FILTHY
Los Angeles District Office (LOS-DO)
4/3/2007
07BGT99FRIED SNACK FOODS, N.E.C.
249FILTHY
Los Angeles District Office (LOS-DO)
4/3/2007
29ACT99NONCARBONATED SOFT DRINK, N.E.C.
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is K.K. International's FDA import refusal history?

K.K. International (FEI: 3005213464) has 4 FDA import refusal record(s) in our database, spanning from 4/3/2007 to 4/3/2007.

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.K. International's FEI number is 3005213464.

What types of violations has K.K. International received?

K.K. International 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 K.K. International come from?

All FDA import refusal data for K.K. International 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.