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Tenczynek Zaklad Przetworstwa

⚠️ Moderate Risk

FEI: 3004769555 • Krzeszowice, Malopolskie • POLAND

FEI

FEI Number

3004769555

📍

Location

Krzeszowice, Malopolskie

🇵🇱

Country

POLAND
🏢

Address

Ulica Tenczynska 1, , Krzeszowice, Malopolskie, Poland

Moderate Risk

FDA Import Risk Assessment

49.5
LowModerateHighCritical

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

Statistics

15
Total Refusals
6
Unique Violations
6/21/2006
Latest Refusal
6/30/2005
Earliest Refusal

Score Breakdown

Violation Severity
65.2×40%
Refusal Volume
44.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

835×

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.

114×

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).

2184×

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.

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).

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)).

4821×

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.

Refusal History

DateProductViolationsDivision
6/21/2006
25RCP02TRUFFLE, BROKEN OR KIBBLED
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
6/21/2006
25RCP02TRUFFLE, BROKEN OR KIBBLED
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
6/21/2006
24KCE20CUCUMBERS, WITH SAUCE
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
6/21/2006
25YCE99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C.
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/25/2006
33SMT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
324NO ENGLISH
Los Angeles District Office (LOS-DO)
5/25/2006
27YGT06PEPPER SAUCE (HOT, MILD, ETC.)
218LIST INGRE
Los Angeles District Office (LOS-DO)
5/25/2006
27YGT06PEPPER SAUCE (HOT, MILD, ETC.)
218LIST INGRE
Los Angeles District Office (LOS-DO)
5/25/2006
27YGT06PEPPER SAUCE (HOT, MILD, ETC.)
218LIST INGRE
Los Angeles District Office (LOS-DO)
5/24/2006
33SFT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
11UNSAFE COL
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
5/24/2006
33SFT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
11UNSAFE COL
324NO ENGLISH
Los Angeles District Office (LOS-DO)
5/24/2006
33SMT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)
5/24/2006
33SMT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)
5/23/2006
29WGY99WATER AND ICE, N.E.C.
324NO ENGLISH
Los Angeles District Office (LOS-DO)
5/23/2006
37JCT08TOMATO SAUCE (WITH OTHER INGREDIENTS)
218LIST INGRE
Los Angeles District Office (LOS-DO)
6/30/2005
38BME99CONCENTRATED SOUP, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Tenczynek Zaklad Przetworstwa's FDA import refusal history?

Tenczynek Zaklad Przetworstwa (FEI: 3004769555) has 15 FDA import refusal record(s) in our database, spanning from 6/30/2005 to 6/21/2006.

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. Tenczynek Zaklad Przetworstwa's FEI number is 3004769555.

What types of violations has Tenczynek Zaklad Przetworstwa received?

Tenczynek Zaklad Przetworstwa 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 Tenczynek Zaklad Przetworstwa come from?

All FDA import refusal data for Tenczynek Zaklad Przetworstwa 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.