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Spartacus Leather

⚠️ Moderate Risk

FEI: 3010531683 • Milwaukie, WI • UNITED STATES

FEI

FEI Number

3010531683

📍

Location

Milwaukie, WI

🇺🇸
🏢

Address

4287 Se International Way Ste D, , Milwaukie, WI, United States

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

4
Total Refusals
6
Unique Violations
4/21/2015
Latest Refusal
1/16/2014
Earliest Refusal

Score Breakdown

Violation Severity
63.3×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
31.7×10%
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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

2371×

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).

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
4/21/2015
89IROVIBRATOR, THERAPEUTIC
508NO 510(K)
New Orleans District Office (NOL-DO)
4/6/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
223FALSE
New Orleans District Office (NOL-DO)
2/23/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
New Orleans District Office (NOL-DO)
1/16/2014
78LSTDEVICE, ERECTILE DYSFUNCTION
16DIRECTIONS
237NO PMA
3280FRNMFGREG
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Spartacus Leather's FDA import refusal history?

Spartacus Leather (FEI: 3010531683) has 4 FDA import refusal record(s) in our database, spanning from 1/16/2014 to 4/21/2015.

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. Spartacus Leather's FEI number is 3010531683.

What types of violations has Spartacus Leather received?

Spartacus Leather has been cited for 6 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 Spartacus Leather come from?

All FDA import refusal data for Spartacus Leather 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.