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"PIONIR" D.O.O. BEOGRAD "FABRIKA SUBOTICA"

⚠️ Moderate Risk

FEI: 3011114040 • Subotica, Subotica • SERBIA

FEI

FEI Number

3011114040

📍

Location

Subotica, Subotica

🇷🇸

Country

SERBIA
🏢

Address

Sencanski Put 83, , Subotica, Subotica, Serbia

Moderate Risk

FDA Import Risk Assessment

30.4
LowModerateHighCritical

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

Statistics

4
Total Refusals
6
Unique Violations
5/20/2002
Latest Refusal
5/20/2002
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
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

2563×

INCONSPICU

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)).

642×

YELLOW #5

The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.

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).

2551×

STD FILL

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(h)(2) of the FD&C Act in that the article purports to be or is represented as a food for which a standard or standards of fill of container have been prescribed by regulations as provided by Section 401 of the FD&C Act and the article falls below the applicable standard of fill and its label does not bear a statement that it falls below such standard in such manner and form as such regulations specify.

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

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)).

Refusal History

DateProductViolationsDivision
5/20/2002
34BFT09MILK CHOCOLATE, SWEET MILK CHOCOLATE AND COATING (EXCEPT CHOCOLATE CANDY AND CHOCOLATE BEVERAGE BASE
256INCONSPICU
324NO ENGLISH
Cincinnati District Office (CIN-DO)
5/20/2002
03EGB99DOUGHS FOR BREAD,ROLLS,MUFFINS, AND BUNS, N.E.C.
256INCONSPICU
Cincinnati District Office (CIN-DO)
5/20/2002
34BFT09MILK CHOCOLATE, SWEET MILK CHOCOLATE AND COATING (EXCEPT CHOCOLATE CANDY AND CHOCOLATE BEVERAGE BASE
255STD FILL
64YELLOW #5
Cincinnati District Office (CIN-DO)
5/20/2002
33EGB06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
256INCONSPICU
260FALSE
64YELLOW #5
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is "PIONIR" D.O.O. BEOGRAD "FABRIKA SUBOTICA"'s FDA import refusal history?

"PIONIR" D.O.O. BEOGRAD "FABRIKA SUBOTICA" (FEI: 3011114040) has 4 FDA import refusal record(s) in our database, spanning from 5/20/2002 to 5/20/2002.

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. "PIONIR" D.O.O. BEOGRAD "FABRIKA SUBOTICA"'s FEI number is 3011114040.

What types of violations has "PIONIR" D.O.O. BEOGRAD "FABRIKA SUBOTICA" received?

"PIONIR" D.O.O. BEOGRAD "FABRIKA SUBOTICA" 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 "PIONIR" D.O.O. BEOGRAD "FABRIKA SUBOTICA" come from?

All FDA import refusal data for "PIONIR" D.O.O. BEOGRAD "FABRIKA SUBOTICA" 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.