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STGT SR3

⚠️ Moderate Risk

FEI: 3019798835 • Surat, Thani • THAILAND

FEI

FEI Number

3019798835

📍

Location

Surat, Thani

🇹🇭

Country

THAILAND
🏢

Address

110/19 Ban Khao Mai Daeng, Moo 7, Phlai Wat, Kanchaanadit, Surat, Thani, Thailand

Moderate Risk

FDA Import Risk Assessment

31.6
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
8/9/2022
Latest Refusal
8/9/2022
Earliest Refusal

Score Breakdown

Violation Severity
52.5×40%
Refusal Volume
11.2×30%
Recency
31.5×20%
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).

20201×

LBLG ADVER

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded because its labeling is misleading in a particular, namely that it fails to reveal facts (non-sterility) that are material with respect to consequences which may result from the use of the article according to the labeling, or advertising, or under such conditions of use as are customary or usual.

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.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
8/9/2022
80LYYGLOVE, PATIENT EXAMINATION, LATEX
118NOT LISTED
2020LBLG ADVER
3280FRNMFGREG
333LACKS FIRM
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is STGT SR3's FDA import refusal history?

STGT SR3 (FEI: 3019798835) has 1 FDA import refusal record(s) in our database, spanning from 8/9/2022 to 8/9/2022.

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. STGT SR3's FEI number is 3019798835.

What types of violations has STGT SR3 received?

STGT SR3 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 STGT SR3 come from?

All FDA import refusal data for STGT SR3 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.