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VISPAK d.d.

⚠️ Moderate Risk

FEI: 3003003576 • Visoko, Federacija Bosne i Hercegovine • BOSNIA AND HERZEGOVINA

FEI

FEI Number

3003003576

📍

Location

Visoko, Federacija Bosne i Hercegovine

🇧🇦
🏢

Address

Ozrakovici Bb, , Visoko, Federacija Bosne i Hercegovine, Bosnia and Herzegovina

Moderate Risk

FDA Import Risk Assessment

39.5
LowModerateHighCritical

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

Statistics

10
Total Refusals
8
Unique Violations
1/30/2020
Latest Refusal
2/7/2005
Earliest Refusal

Score Breakdown

Violation Severity
68.1×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
6.7×10%
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

627×

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).

837×

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.

4822×

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.

3241×

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)).

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

3281×

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.

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.

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.

Refusal History

DateProductViolationsDivision
1/30/2020
24VCI04BEET TOPS, WITH SAUCE
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
1/30/2020
24KCI20CUCUMBERS, WITH SAUCE
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
1/30/2020
24HCI04PIMIENTO PEPPER, DRIED OR PASTE
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
1/30/2020
24KCI07PEPPER, SWEET, WITH SAUCE
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
1/30/2020
24KCI07PEPPER, SWEET, WITH SAUCE
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
1/30/2020
24KCI07PEPPER, SWEET, WITH SAUCE
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
1/30/2020
24KCI07PEPPER, SWEET, WITH SAUCE
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
4/22/2014
02DGT02RICE, PLAIN (WHITE OR POLISHED) PROCESSED (PACKAGED)
218LIST INGRE
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
New York District Office (NYK-DO)
3/14/2005
35AGT01GELATIN, FLAVORED
11UNSAFE COL
New York District Office (NYK-DO)
2/7/2005
33GGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITH NUTS OR NUT PRODUCTS (WITHOUT CHOCOLATE)
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is VISPAK d.d.'s FDA import refusal history?

VISPAK d.d. (FEI: 3003003576) has 10 FDA import refusal record(s) in our database, spanning from 2/7/2005 to 1/30/2020.

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. VISPAK d.d.'s FEI number is 3003003576.

What types of violations has VISPAK d.d. received?

VISPAK d.d. has been cited for 8 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 VISPAK d.d. come from?

All FDA import refusal data for VISPAK d.d. 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.