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Gillette Poland S.A.

✅ Low Risk

FEI: 3011080516 • Lodz, Lodzkie • POLAND

FEI

FEI Number

3011080516

📍

Location

Lodz, Lodzkie

🇵🇱

Country

POLAND
🏢

Address

Ul. Wodna 90/024, 11-13ZIP CODE, Lodz, Lodzkie, Poland

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
1
Unique Violations
1/20/2015
Latest Refusal
1/20/2015
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
1/20/2015
62WAJ99ASTRINGENT/ANTI-PERSPIRANT N.E.C.
3280FRNMFGREG
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Gillette Poland S.A.'s FDA import refusal history?

Gillette Poland S.A. (FEI: 3011080516) has 1 FDA import refusal record(s) in our database, spanning from 1/20/2015 to 1/20/2015.

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. Gillette Poland S.A.'s FEI number is 3011080516.

What types of violations has Gillette Poland S.A. received?

Gillette Poland S.A. has been cited for 1 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 Gillette Poland S.A. come from?

All FDA import refusal data for Gillette Poland S.A. 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.