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ARKRAY, Inc.

⚠️ Moderate Risk

FEI: 3002807423 • Kyoto, Kyoto • JAPAN

FEI

FEI Number

3002807423

📍

Location

Kyoto, Kyoto

🇯🇵

Country

JAPAN
🏢

Address

Kamigyo 59, Gansuin-Cho; Kamigyo, Kyoto, Kyoto, Japan

Moderate Risk

FDA Import Risk Assessment

29.1
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
9/2/2022
Latest Refusal
7/22/2002
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
17.7×30%
Recency
18.4×20%
Frequency
1.0×10%
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

1182×

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).

3411×

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).

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
9/2/2022
73BTYCALCULATOR, PREDICTED VALUES, PULMONARY FUNCTION
118NOT LISTED
341REGISTERED
Division of Southeast Imports (DSEI)
7/22/2002
81GKLCOUNTER, CELL, AUTOMATED (PARTICLE COUNTER)
118NOT LISTED
508NO 510(K)
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is ARKRAY, Inc.'s FDA import refusal history?

ARKRAY, Inc. (FEI: 3002807423) has 2 FDA import refusal record(s) in our database, spanning from 7/22/2002 to 9/2/2022.

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. ARKRAY, Inc.'s FEI number is 3002807423.

What types of violations has ARKRAY, Inc. received?

ARKRAY, Inc. 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 ARKRAY, Inc. come from?

All FDA import refusal data for ARKRAY, Inc. 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.