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SGMP Company Limited

⚠️ Moderate Risk

FEI: 3003069816 • Songkhla • THAILAND

FEI

FEI Number

3003069816

📍

Location

Songkhla

🇹🇭

Country

THAILAND
🏢

Address

181 Moo 6, Tambol Kampaengphet, Amphur Rattaphum, Songkhla, , Thailand

Moderate Risk

FDA Import Risk Assessment

36.4
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
2/25/2019
Latest Refusal
8/22/2012
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
6.1×10%
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

4774×

HOLES

The quality of the article falls below that which it purports or is represented to possess, in that the devices contain defects/holes.

Refusal History

DateProductViolationsDivision
2/25/2019
80LYYGLOVE, PATIENT EXAMINATION, LATEX
477HOLES
Division of Southeast Imports (DSEI)
1/15/2013
80LZCGLOVE, PATIENT EXAMINATION, SPECIALTY
477HOLES
Los Angeles District Office (LOS-DO)
8/22/2012
80LZCGLOVE, PATIENT EXAMINATION, SPECIALTY
477HOLES
Division of Southeast Imports (DSEI)
8/22/2012
80LZCGLOVE, PATIENT EXAMINATION, SPECIALTY
477HOLES
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SGMP Company Limited's FDA import refusal history?

SGMP Company Limited (FEI: 3003069816) has 4 FDA import refusal record(s) in our database, spanning from 8/22/2012 to 2/25/2019.

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. SGMP Company Limited's FEI number is 3003069816.

What types of violations has SGMP Company Limited received?

SGMP Company Limited 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 SGMP Company Limited come from?

All FDA import refusal data for SGMP Company Limited 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.