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Bayer

⚠️ Moderate Risk

FEI: 3008089718 • Warsaw, Mazowieckie • POLAND

FEI

FEI Number

3008089718

📍

Location

Warsaw, Mazowieckie

🇵🇱

Country

POLAND
🏢

Address

Ul. Aleje Jerozolimskie 158, , Warsaw, Mazowieckie, Poland

Moderate Risk

FDA Import Risk Assessment

46.6
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
3/7/2025
Latest Refusal
6/19/2012
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
22.3×30%
Recency
78.5×20%
Frequency
2.4×10%
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

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

3421×

PERSONALRX

The article appears to be a drug which requires a prescription from your doctor.

4721×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
3/7/2025
66XDB05HOMEOPATHIC GASTROINTESTINAL
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/17/2020
64GDY29LEVONORGESTREL (ESTROGEN)
118NOT LISTED
342PERSONALRX
Division of Southeast Imports (DSEI)
6/19/2012
60SBY99ANTACID, N.E.C.
118NOT LISTED
16DIRECTIONS
472NO ENGLISH
New York District Office (NYK-DO)

Frequently Asked Questions

What is Bayer's FDA import refusal history?

Bayer (FEI: 3008089718) has 3 FDA import refusal record(s) in our database, spanning from 6/19/2012 to 3/7/2025.

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. Bayer's FEI number is 3008089718.

What types of violations has Bayer received?

Bayer has been cited for 5 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 Bayer come from?

All FDA import refusal data for Bayer 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.