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BUL VITA

⚠️ Moderate Risk

FEI: 3009951690 • Varna, Varna • BULGARIA

FEI

FEI Number

3009951690

📍

Location

Varna, Varna

🇧🇬

Country

BULGARIA
🏢

Address

Oborishte Str. 38, , Varna, Varna, Bulgaria

Moderate Risk

FDA Import Risk Assessment

39.0
LowModerateHighCritical

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

Statistics

10
Total Refusals
4
Unique Violations
3/29/2022
Latest Refusal
1/30/2004
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
38.6×30%
Recency
24.2×20%
Frequency
5.5×10%
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

3214×

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.

3244×

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)).

624×

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).

834×

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
3/29/2022
07AGT02CORN CHIPS, BAKED
321LACKS N/C
324NO ENGLISH
Division of Northern Border Imports (DNBI)
3/29/2022
07AGT02CORN CHIPS, BAKED
321LACKS N/C
324NO ENGLISH
Division of Northern Border Imports (DNBI)
3/29/2022
07AGT02CORN CHIPS, BAKED
321LACKS N/C
324NO ENGLISH
Division of Northern Border Imports (DNBI)
3/29/2022
07AGT02CORN CHIPS, BAKED
321LACKS N/C
324NO ENGLISH
Division of Northern Border Imports (DNBI)
4/6/2006
24KCI07PEPPER, SWEET, WITH SAUCE
83NO PROCESS
New York District Office (NYK-DO)
3/22/2006
24FCE08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
3/22/2006
24FCE08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
2/25/2004
24FCE08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
83NO PROCESS
New York District Office (NYK-DO)
1/30/2004
24FCE08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
62NEEDS FCE
New York District Office (NYK-DO)
1/30/2004
27YCE99CONDIMENTS, N.E.C.
62NEEDS FCE
New York District Office (NYK-DO)

Frequently Asked Questions

What is BUL VITA's FDA import refusal history?

BUL VITA (FEI: 3009951690) has 10 FDA import refusal record(s) in our database, spanning from 1/30/2004 to 3/29/2022.

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. BUL VITA's FEI number is 3009951690.

What types of violations has BUL VITA received?

BUL VITA has been cited for 4 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 BUL VITA come from?

All FDA import refusal data for BUL VITA 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.