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UPS DEUTSCHLAND INC CO OHG

⚠️ Moderate Risk

FEI: 3012366537 • Cologne • GERMANY

FEI

FEI Number

3012366537

📍

Location

Cologne

🇩🇪

Country

GERMANY
🏢

Address

Heinrich Steinmann Stra, , Cologne, , Germany

Moderate Risk

FDA Import Risk Assessment

42.1
LowModerateHighCritical

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

Statistics

2
Total Refusals
5
Unique Violations
4/18/2025
Latest Refusal
9/18/2019
Earliest Refusal

Score Breakdown

Violation Severity
56.0×40%
Refusal Volume
17.7×30%
Recency
70.2×20%
Frequency
3.6×10%
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

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.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

471×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

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
4/18/2025
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
47NON STD
Division of Southeast Imports (DSEI)
9/18/2019
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is UPS DEUTSCHLAND INC CO OHG's FDA import refusal history?

UPS DEUTSCHLAND INC CO OHG (FEI: 3012366537) has 2 FDA import refusal record(s) in our database, spanning from 9/18/2019 to 4/18/2025.

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. UPS DEUTSCHLAND INC CO OHG's FEI number is 3012366537.

What types of violations has UPS DEUTSCHLAND INC CO OHG received?

UPS DEUTSCHLAND INC CO OHG 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 UPS DEUTSCHLAND INC CO OHG come from?

All FDA import refusal data for UPS DEUTSCHLAND INC CO OHG 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.