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A-Grosik Przetworstwo Spozywcze I Handel

⚠️ Moderate Risk

FEI: 3001812048 • Warsaw, Mazowieckie • POLAND

FEI

FEI Number

3001812048

📍

Location

Warsaw, Mazowieckie

🇵🇱

Country

POLAND
🏢

Address

Ul. Piwna 51/53, , Warsaw, Mazowieckie, Poland

Moderate Risk

FDA Import Risk Assessment

36.2
LowModerateHighCritical

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

Statistics

4
Total Refusals
6
Unique Violations
12/20/2013
Latest Refusal
2/27/2004
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
4.1×10%
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

2381×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

29201×

PESTICIDES

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

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.

621×

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).

831×

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
12/20/2013
24FCI20CUCUMBERS (FRUIT USED AS VEGETABLE)
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
12/6/2005
20ECE08GOOSEBERRY, TOPPING OR SYRUP
2920PESTICIDES
Chicago District Office (CHI-DO)
12/6/2005
25LCE08RED BEET, DRIED OR PASTE
62NEEDS FCE
83NO PROCESS
Chicago District Office (CHI-DO)
2/27/2004
20ACE08GOOSEBERRIES (BERRY)
238UNSAFE ADD
Detroit District Office (DET-DO)

Frequently Asked Questions

What is A-Grosik Przetworstwo Spozywcze I Handel's FDA import refusal history?

A-Grosik Przetworstwo Spozywcze I Handel (FEI: 3001812048) has 4 FDA import refusal record(s) in our database, spanning from 2/27/2004 to 12/20/2013.

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. A-Grosik Przetworstwo Spozywcze I Handel's FEI number is 3001812048.

What types of violations has A-Grosik Przetworstwo Spozywcze I Handel received?

A-Grosik Przetworstwo Spozywcze I Handel 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 A-Grosik Przetworstwo Spozywcze I Handel come from?

All FDA import refusal data for A-Grosik Przetworstwo Spozywcze I Handel 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.