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Xgen Products

⚠️ Moderate Risk

FEI: 3010628001 • Horsham, PA • UNITED STATES

FEI

FEI Number

3010628001

📍

Location

Horsham, PA

🇺🇸
🏢

Address

201 Precision Rd, , Horsham, PA, United States

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
8/29/2016
Latest Refusal
8/29/2016
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

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.

5081×

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.

Refusal History

DateProductViolationsDivision
8/29/2016
85PEBLUBRICANT, PERSONAL, GAMETE, FERTILIZATION, AND EMBRYO COMPATIBLE
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Xgen Products's FDA import refusal history?

Xgen Products (FEI: 3010628001) has 1 FDA import refusal record(s) in our database, spanning from 8/29/2016 to 8/29/2016.

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. Xgen Products's FEI number is 3010628001.

What types of violations has Xgen Products received?

Xgen Products has been cited for 2 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 Xgen Products come from?

All FDA import refusal data for Xgen Products 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.