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NUMTALSOD STERILIZE PART

⚠️ Moderate Risk

FEI: 3010140518 • Bang Khonthi, Samut Songkhram • THAILAND

FEI

FEI Number

3010140518

📍

Location

Bang Khonthi, Samut Songkhram

🇹🇭

Country

THAILAND
🏢

Address

Moo 4, 15 Donmanora, Bang Khonthi, Samut Songkhram, Thailand

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/5/2009
Latest Refusal
11/5/2009
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
11/5/2009
21VCT24PALM NUT (PALM FRUIT, SUGAR PALM), JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is NUMTALSOD STERILIZE PART's FDA import refusal history?

NUMTALSOD STERILIZE PART (FEI: 3010140518) has 1 FDA import refusal record(s) in our database, spanning from 11/5/2009 to 11/5/2009.

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. NUMTALSOD STERILIZE PART's FEI number is 3010140518.

What types of violations has NUMTALSOD STERILIZE PART received?

NUMTALSOD STERILIZE PART has been cited for 1 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 NUMTALSOD STERILIZE PART come from?

All FDA import refusal data for NUMTALSOD STERILIZE PART 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.