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Overnight Euro Exp

⚠️ Moderate Risk

FEI: 3010791544 • Luxembourg • LUXEMBOURG

FEI

FEI Number

3010791544

📍

Location

Luxembourg

🇱🇺

Country

LUXEMBOURG
🏢

Address

66 Rue Des Celtes, , Luxembourg, , Luxembourg

Moderate Risk

FDA Import Risk Assessment

39.5
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
12/14/2021
Latest Refusal
12/14/2021
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
25.9×30%
Recency
18.4×20%
Frequency
40.0×10%
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

1184×

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).

32804×

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.

5084×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

2372×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

Refusal History

DateProductViolationsDivision
12/14/2021
80QOZBARRIER FACE COVERING PER ENFORCEMENT POLICY FOR FACE MASKS AND RESPIRATORS DURING THE COVID-19 PUBL
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
12/14/2021
80QOZBARRIER FACE COVERING PER ENFORCEMENT POLICY FOR FACE MASKS AND RESPIRATORS DURING THE COVID-19 PUBL
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
12/14/2021
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
12/14/2021
83QKPCORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Overnight Euro Exp's FDA import refusal history?

Overnight Euro Exp (FEI: 3010791544) has 4 FDA import refusal record(s) in our database, spanning from 12/14/2021 to 12/14/2021.

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. Overnight Euro Exp's FEI number is 3010791544.

What types of violations has Overnight Euro Exp received?

Overnight Euro Exp has been cited for 4 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 Overnight Euro Exp come from?

All FDA import refusal data for Overnight Euro Exp 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.