ImportRefusal LogoImportRefusal

Fdx Customs

⚠️ Moderate Risk

FEI: 3002899974 • Roissy-En-France, Val-d'Oise • FRANCE

FEI

FEI Number

3002899974

📍

Location

Roissy-En-France, Val-d'Oise

🇫🇷

Country

FRANCE
🏢

Address

Street, , Roissy-En-France, Val-d'Oise, France

Moderate Risk

FDA Import Risk Assessment

39.7
LowModerateHighCritical

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

Statistics

4
Total Refusals
3
Unique Violations
1/4/2005
Latest Refusal
5/14/2002
Earliest Refusal

Score Breakdown

Violation Severity
76.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
15.1×10%
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

1792×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

752×

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).

271×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

Refusal History

DateProductViolationsDivision
1/4/2005
60NCY14TESTOSTERONE (ANDROGEN)
27DRUG GMPS
75UNAPPROVED
New Orleans District Office (NOL-DO)
2/23/2004
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
8/15/2003
64GKY99ESTROGEN N.E.C.
179AGR RX
New Orleans District Office (NOL-DO)
5/14/2002
65PCA02SILDENAFIL CITRATE (REGULATOR)
179AGR RX
New York District Office (NYK-DO)

Frequently Asked Questions

What is Fdx Customs's FDA import refusal history?

Fdx Customs (FEI: 3002899974) has 4 FDA import refusal record(s) in our database, spanning from 5/14/2002 to 1/4/2005.

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. Fdx Customs's FEI number is 3002899974.

What types of violations has Fdx Customs received?

Fdx Customs has been cited for 3 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 Fdx Customs come from?

All FDA import refusal data for Fdx Customs 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.