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Griffith Laboratories

⚠️ Moderate Risk

FEI: 3001598116 • Bangkok • THAILAND

FEI

FEI Number

3001598116

📍

Location

Bangkok

🇹🇭

Country

THAILAND
🏢

Address

Unknown Street, , Bangkok, , Thailand

Moderate Risk

FDA Import Risk Assessment

45.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
2/22/2007
Latest Refusal
11/8/2005
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
23.3×10%
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

113×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

Refusal History

DateProductViolationsDivision
2/22/2007
28KGT99SPICES AND SEASONING, GROUND, CRACKED, WITH SALT, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
1/29/2007
28KGT99SPICES AND SEASONING, GROUND, CRACKED, WITH SALT, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
11/8/2005
28KGT99SPICES AND SEASONING, GROUND, CRACKED, WITH SALT, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Griffith Laboratories's FDA import refusal history?

Griffith Laboratories (FEI: 3001598116) has 3 FDA import refusal record(s) in our database, spanning from 11/8/2005 to 2/22/2007.

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. Griffith Laboratories's FEI number is 3001598116.

What types of violations has Griffith Laboratories received?

Griffith Laboratories 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 Griffith Laboratories come from?

All FDA import refusal data for Griffith Laboratories 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.