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Final Plast D.O.O

⚠️ Moderate Risk

FEI: 3031464911 • Skopje, MK-85 • MACEDONIA

FEI

FEI Number

3031464911

📍

Location

Skopje, MK-85

🇲🇰

Country

MACEDONIA
🏢

Address

Boris Trajkovski Br.75/Kompl.Ohis, , Skopje, MK-85, Macedonia

Moderate Risk

FDA Import Risk Assessment

48.3
LowModerateHighCritical

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

Statistics

6
Total Refusals
7
Unique Violations
10/30/2025
Latest Refusal
10/30/2025
Earliest Refusal

Score Breakdown

Violation Severity
34.4×40%
Refusal Volume
31.3×30%
Recency
96.0×20%
Frequency
60.0×10%
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

4826×

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.

3216×

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.

3283×

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.

3243×

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)).

3203×

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.

3291×

JUICE %

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 the food purports to be a beverage containing vegetable or fruit juice and does not bear a statement on the label in appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained therein.

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.

Refusal History

DateProductViolationsDivision
10/30/2025
24HGT07PEPPER, SWEET, DRIED OR PASTE
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
10/30/2025
24HGT08PEPPER, HOT, DRIED OR PASTE
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
10/30/2025
07BYT06POTATO CHIPS,FRIED
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
10/30/2025
29WGY02BOTTLED SPRING OR MINERAL WATER
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
10/30/2025
21KFY13PEACH, JUICE, PIT FRUIT JUICES OR CONCENTRATES
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
329JUICE %
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
10/30/2025
20DFY14STRAWBERRY JUICE, BERRY JUICE OR CONCENTRATES
218LIST INGRE
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Final Plast D.O.O's FDA import refusal history?

Final Plast D.O.O (FEI: 3031464911) has 6 FDA import refusal record(s) in our database, spanning from 10/30/2025 to 10/30/2025.

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. Final Plast D.O.O's FEI number is 3031464911.

What types of violations has Final Plast D.O.O received?

Final Plast D.O.O has been cited for 7 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 Final Plast D.O.O come from?

All FDA import refusal data for Final Plast D.O.O 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.