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OKAMOTO RUBBER PRODUCTS CO., LTD

⚠️ Moderate Risk

FEI: 3012513722 • Pathum Thani • THAILAND

FEI

FEI Number

3012513722

📍

Location

Pathum Thani

🇹🇭

Country

THAILAND
🏢

Address

60/50, 60/51 Soi 13 Moo, Estate Zone, Klongnueng, Klonglu, Pathum Thani, , Thailand

Moderate Risk

FDA Import Risk Assessment

40.4
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
8/2/2024
Latest Refusal
9/30/2017
Earliest Refusal

Score Breakdown

Violation Severity
51.8×40%
Refusal Volume
25.9×30%
Recency
56.4×20%
Frequency
5.8×10%
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

1184×

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).

5083×

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.

32802×

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.

3412×

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).

Refusal History

DateProductViolationsDivision
8/2/2024
85NUCLUBRICANT, PATIENT, VAGINAL, LATEX COMPATIBLE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
8/2/2024
85HISCONDOM
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)
9/30/2017
85HISCONDOM
118NOT LISTED
508NO 510(K)
Division of Northeast Imports (DNEI)
9/30/2017
85HISCONDOM
118NOT LISTED
508NO 510(K)
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is OKAMOTO RUBBER PRODUCTS CO., LTD's FDA import refusal history?

OKAMOTO RUBBER PRODUCTS CO., LTD (FEI: 3012513722) has 4 FDA import refusal record(s) in our database, spanning from 9/30/2017 to 8/2/2024.

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. OKAMOTO RUBBER PRODUCTS CO., LTD's FEI number is 3012513722.

What types of violations has OKAMOTO RUBBER PRODUCTS CO., LTD received?

OKAMOTO RUBBER PRODUCTS 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 OKAMOTO RUBBER PRODUCTS CO., LTD come from?

All FDA import refusal data for OKAMOTO RUBBER PRODUCTS 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.