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Green Spot

⚠️ Moderate Risk

FEI: 3017392438 • Nong Khae, TH-19 • THAILAND

FEI

FEI Number

3017392438

📍

Location

Nong Khae, TH-19

🇹🇭

Country

THAILAND
🏢

Address

28 Moo 1, Nong Khae Industrial Estate, Nong Khai Nam, Nong Khae, TH-19, Thailand

Moderate Risk

FDA Import Risk Assessment

45.4
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
10/21/2024
Latest Refusal
5/3/2024
Earliest Refusal

Score Breakdown

Violation Severity
48.9×40%
Refusal Volume
28.8×30%
Recency
61.0×20%
Frequency
50.0×10%
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

4825×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

23002×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

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
10/21/2024
29AFT99NONCARBONATED SOFT DRINK, N.E.C.
482NUTRIT LBL
Division of Northeast Imports (DNEI)
8/16/2024
14BCT01IMITATION MILK, FLUID MILK TYPE PRODUCT
2300DIETARYLBL
482NUTRIT LBL
Division of Northeast Imports (DNEI)
8/16/2024
14BCT01IMITATION MILK, FLUID MILK TYPE PRODUCT
2300DIETARYLBL
482NUTRIT LBL
Division of Northeast Imports (DNEI)
6/11/2024
29CCY04MIXED DRINKS (NONALCOHOLIC BEVERAGES)
482NUTRIT LBL
Division of Northeast Imports (DNEI)
5/3/2024
09CCY26MILK AND MILK PRODUCTS, CULTURED OR ACIDIFIED
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Green Spot's FDA import refusal history?

Green Spot (FEI: 3017392438) has 5 FDA import refusal record(s) in our database, spanning from 5/3/2024 to 10/21/2024.

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. Green Spot's FEI number is 3017392438.

What types of violations has Green Spot received?

Green Spot 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 Green Spot come from?

All FDA import refusal data for Green Spot 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.