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Konex-Tiva Ltd

⚠️ Moderate Risk

FEI: 3003072133 • Sofiya, Oblast Sofiya Grad • BULGARIA

FEI

FEI Number

3003072133

📍

Location

Sofiya, Oblast Sofiya Grad

🇧🇬

Country

BULGARIA
🏢

Address

Bulevard Bilgariya 9, , Sofiya, Oblast Sofiya Grad, Bulgaria

Moderate Risk

FDA Import Risk Assessment

37.7
LowModerateHighCritical

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

Statistics

10
Total Refusals
6
Unique Violations
12/20/2013
Latest Refusal
1/5/2004
Earliest Refusal

Score Breakdown

Violation Severity
62.9×40%
Refusal Volume
38.6×30%
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

4825×

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.

29203×

PESTICIDES

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

2382×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

832×

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.

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.

4731×

LABELING

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

Refusal History

DateProductViolationsDivision
12/20/2013
24KCI07PEPPER, SWEET, WITH SAUCE
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
12/28/2012
24FCI07PEPPER, SWEET (FRUIT USED AS VEGETABLE)
83NO PROCESS
New York District Office (NYK-DO)
4/12/2006
21LCT03CHERRY, TOPPING OR SYRUP
2920PESTICIDES
Chicago District Office (CHI-DO)
8/1/2005
24FCI20CUCUMBERS (FRUIT USED AS VEGETABLE)
482NUTRIT LBL
New York District Office (NYK-DO)
4/12/2005
24FCI08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
482NUTRIT LBL
83NO PROCESS
New York District Office (NYK-DO)
1/26/2005
25QCI99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C.
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
12/15/2004
21GCT03CHERRY FRUIT (PIT FRUIT)
2920PESTICIDES
Detroit District Office (DET-DO)
12/15/2004
21GCT03CHERRY FRUIT (PIT FRUIT)
2920PESTICIDES
Detroit District Office (DET-DO)
6/25/2004
21GCP03CHERRY FRUIT (PIT FRUIT)
238UNSAFE ADD
Southwest Import District Office (SWI-DO)
1/5/2004
21GCT03CHERRY FRUIT (PIT FRUIT)
238UNSAFE ADD
482NUTRIT LBL
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Konex-Tiva Ltd's FDA import refusal history?

Konex-Tiva Ltd (FEI: 3003072133) has 10 FDA import refusal record(s) in our database, spanning from 1/5/2004 to 12/20/2013.

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. Konex-Tiva Ltd's FEI number is 3003072133.

What types of violations has Konex-Tiva Ltd received?

Konex-Tiva Ltd 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 Konex-Tiva Ltd come from?

All FDA import refusal data for Konex-Tiva Ltd 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.