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NAKANISHI OPTICAL PRODUCTS

✅ Low Risk

FEI: 3012585381 • Umeda, Osaka • JAPAN

FEI

FEI Number

3012585381

📍

Location

Umeda, Osaka

🇯🇵

Country

JAPAN
🏢

Address

1 Osaka Ekimae Bldg3 1, , Umeda, Osaka, Japan

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
1
Unique Violations
11/1/2017
Latest Refusal
11/1/2017
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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.

Refusal History

DateProductViolationsDivision
11/1/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is NAKANISHI OPTICAL PRODUCTS's FDA import refusal history?

NAKANISHI OPTICAL PRODUCTS (FEI: 3012585381) has 1 FDA import refusal record(s) in our database, spanning from 11/1/2017 to 11/1/2017.

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. NAKANISHI OPTICAL PRODUCTS's FEI number is 3012585381.

What types of violations has NAKANISHI OPTICAL PRODUCTS received?

NAKANISHI OPTICAL PRODUCTS has been cited for 1 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 NAKANISHI OPTICAL PRODUCTS come from?

All FDA import refusal data for NAKANISHI OPTICAL 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.