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Beiersdorf Manufacturing Hamburg Gmbh

⚠️ Moderate Risk

FEI: 3006653492 • Hamburg, Hamburg • GERMANY

FEI

FEI Number

3006653492

📍

Location

Hamburg, Hamburg

🇩🇪

Country

GERMANY
🏢

Address

Beiersdorfstrasse 2, , Hamburg, Hamburg, Germany

Moderate Risk

FDA Import Risk Assessment

49.3
LowModerateHighCritical

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

Statistics

5
Total Refusals
6
Unique Violations
9/24/2025
Latest Refusal
11/22/2023
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
28.8×30%
Recency
79.7×20%
Frequency
27.2×10%
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

1972×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

38812×

COSMETFPLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an undeclared color additive which renders it misbranded within the meaning of Sections 1454(c)(3)(B) and 1456 of the Fair Packaging and Labeling Act.

1181×

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).

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.

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

Refusal History

DateProductViolationsDivision
9/24/2025
66PAY05HOMOSALATE (ULTRAVIOLET SCREEN/SUNSCREEN)
118NOT LISTED
3280FRNMFGREG
Division of Northeast Imports (DNEI)
12/4/2024
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
471CSTIC LBLG
475COSMETLBLG
Division of Southeast Imports (DSEI)
9/10/2024
53LC06MOISTURIZING (SKIN CARE PREPARATIONS)
197COSM COLOR
Division of Southeast Imports (DSEI)
11/22/2023
53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
3881COSMETFPLA
Division of Northeast Imports (DNEI)
11/22/2023
53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
197COSM COLOR
3881COSMETFPLA
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Beiersdorf Manufacturing Hamburg Gmbh's FDA import refusal history?

Beiersdorf Manufacturing Hamburg Gmbh (FEI: 3006653492) has 5 FDA import refusal record(s) in our database, spanning from 11/22/2023 to 9/24/2025.

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. Beiersdorf Manufacturing Hamburg Gmbh's FEI number is 3006653492.

What types of violations has Beiersdorf Manufacturing Hamburg Gmbh received?

Beiersdorf Manufacturing Hamburg Gmbh 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 Beiersdorf Manufacturing Hamburg Gmbh come from?

All FDA import refusal data for Beiersdorf Manufacturing Hamburg Gmbh 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.