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Nidak Co

⚠️ Moderate Risk

FEI: 3003961660 • Chiyoda-Ku To • JAPAN

FEI

FEI Number

3003961660

📍

Location

Chiyoda-Ku To

🇯🇵

Country

JAPAN
🏢

Address

Kanda-Jinbo-Cho, , Chiyoda-Ku To, , Japan

Moderate Risk

FDA Import Risk Assessment

34.2
LowModerateHighCritical

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

Statistics

12
Total Refusals
5
Unique Violations
6/25/2013
Latest Refusal
11/16/2009
Earliest Refusal

Score Breakdown

Violation Severity
46.2×40%
Refusal Volume
41.3×30%
Recency
0.0×20%
Frequency
33.3×10%
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

34112×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

1188×

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).

5085×

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.

32803×

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.

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).

Refusal History

DateProductViolationsDivision
6/25/2013
86HOSPROJECTOR, OPHTHALMIC
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Florida District Office (FLA-DO)
6/25/2013
86HOSPROJECTOR, OPHTHALMIC
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Florida District Office (FLA-DO)
6/25/2013
86HNOKERATOME, AC-POWERED
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Florida District Office (FLA-DO)
6/25/2013
86HJOBIOMICROSCOPE, SLIT-LAMP, AC-POWERED
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
6/25/2013
86MYCOPHTHALMOSCOPE, LASER, SCANNING
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
6/25/2013
86LQBMEDICAL COMPUTERS AND SOFTWARE FOR OPHTHALMIC USE
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
6/25/2013
86HKICAMERA, OPHTHALMIC, AC-POWERED
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
6/25/2013
86HMCMONITOR, EYE MOVEMENT, DIAGNOSTIC
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
4/16/2013
86HKXTONOMETER, AC-POWERED
341REGISTERED
San Juan District Office (SJN-DO)
11/15/2011
86HQBPHOTOCOAGULATOR AND ACCESSORIES
341REGISTERED
Florida District Office (FLA-DO)
8/25/2011
86HKNREFRACTOR, MANUAL, NON-POWERED, INCLUDING PHOROPTER
341REGISTERED
Detroit District Office (DET-DO)
11/16/2009
86HQLLENS, INTRAOCULAR
237NO PMA
341REGISTERED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Nidak Co's FDA import refusal history?

Nidak Co (FEI: 3003961660) has 12 FDA import refusal record(s) in our database, spanning from 11/16/2009 to 6/25/2013.

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. Nidak Co's FEI number is 3003961660.

What types of violations has Nidak Co received?

Nidak Co has been cited for 5 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 Nidak Co come from?

All FDA import refusal data for Nidak Co 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.