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Aire Inc

⚠️ Moderate Risk

FEI: 3011410259 • Tokyo • JAPAN

FEI

FEI Number

3011410259

📍

Location

Tokyo

🇯🇵

Country

JAPAN
🏢

Address

1- Chrome, No. 33 No.8 Ikebukuro Towe, , Tokyo, , Japan

Moderate Risk

FDA Import Risk Assessment

25.9
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
5/10/2019
Latest Refusal
5/10/2019
Earliest Refusal

Score Breakdown

Violation Severity
54.0×40%
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

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).

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(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.

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
5/10/2019
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3260NO ENGLISH
3280FRNMFGREG
508NO 510(K)
84RX DEVICE
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Aire Inc's FDA import refusal history?

Aire Inc (FEI: 3011410259) has 1 FDA import refusal record(s) in our database, spanning from 5/10/2019 to 5/10/2019.

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. Aire Inc's FEI number is 3011410259.

What types of violations has Aire Inc received?

Aire Inc 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 Aire Inc come from?

All FDA import refusal data for Aire 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.