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Lufthansa Technik

⚠️ Moderate Risk

FEI: 1000611464 • Hamburg, Hamburg • GERMANY

FEI

FEI Number

1000611464

📍

Location

Hamburg, Hamburg

🇩🇪

Country

GERMANY
🏢

Address

Weg Beim Jager 193, , Hamburg, Hamburg, Germany

Moderate Risk

FDA Import Risk Assessment

49.4
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
1/9/2026
Latest Refusal
5/6/2003
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
25.9×30%
Recency
97.1×20%
Frequency
1.8×10%
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

472×

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.

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.

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
1/9/2026
95RHHLED, GENERAL PURPOSE ILLUMINATION, GENERAL OPTICAL PRODUCTS, NON-MEDICAL
47NON STD
Division of Southeast Imports (DSEI)
7/24/2017
89IORWHEELCHAIR, MECHANICAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)
8/30/2005
94V07TV RECEIVER OR PRODUCT CONT. TV RECEIVER, TELEVISION, COMPUTER MONITOR
476NO REGISTR
Cincinnati District Office (CIN-DO)
5/6/2003
95L31CD PLAYERS (COMPACT DISC PLAYERS)
47NON STD
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Lufthansa Technik's FDA import refusal history?

Lufthansa Technik (FEI: 1000611464) has 4 FDA import refusal record(s) in our database, spanning from 5/6/2003 to 1/9/2026.

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. Lufthansa Technik's FEI number is 1000611464.

What types of violations has Lufthansa Technik received?

Lufthansa Technik 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 Lufthansa Technik come from?

All FDA import refusal data for Lufthansa Technik 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.