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JMEC Co., Ltd.

⚠️ Moderate Risk

FEI: 3004429507 • Bunkyo, Tokyo • JAPAN

FEI

FEI Number

3004429507

📍

Location

Bunkyo, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

3 Chome 31-3, Yushima, Bunkyo, Tokyo, Japan

Moderate Risk

FDA Import Risk Assessment

27.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
5/31/2011
Latest Refusal
2/13/2004
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
2.7×10%
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).

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).

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
5/31/2011
53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
3260NO ENGLISH
Southwest Import District Office (SWI-DO)
2/13/2004
89KTBDEVICE, IONTOPHORESIS, SPECIFIC USES
118NOT LISTED
237NO PMA
476NO REGISTR
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is JMEC Co., Ltd.'s FDA import refusal history?

JMEC Co., Ltd. (FEI: 3004429507) has 2 FDA import refusal record(s) in our database, spanning from 2/13/2004 to 5/31/2011.

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. JMEC Co., Ltd.'s FEI number is 3004429507.

What types of violations has JMEC Co., Ltd. received?

JMEC Co., Ltd. has been cited for 4 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 JMEC Co., Ltd. come from?

All FDA import refusal data for JMEC Co., Ltd. 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.