MANOP MEEKHAMKEAW
⚠️ Moderate Risk
FEI: 3013578213 • Chiang Ral • THAILAND
FEI Number
3013578213
Location
Chiang Ral
Country
THAILANDAddress
22, 4 Sol Tetsabam, Chiang Ral, , Thailand
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/27/2018 | 21TVH05MANGO, DRIED OR PASTE | Division of Southeast Imports (DSEI) | |
| 2/27/2018 | 21HVH14PLUM, DRIED OR PASTE | Division of Southeast Imports (DSEI) | |
| 2/27/2018 | 23HVT99MIXED NUTS, SHELLED, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/27/2018 | 28BVH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), GROUND, CRACKED (SPICE) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is MANOP MEEKHAMKEAW's FDA import refusal history?
MANOP MEEKHAMKEAW (FEI: 3013578213) has 4 FDA import refusal record(s) in our database, spanning from 2/27/2018 to 2/27/2018.
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. MANOP MEEKHAMKEAW's FEI number is 3013578213.
What types of violations has MANOP MEEKHAMKEAW received?
MANOP MEEKHAMKEAW has been cited for 2 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 MANOP MEEKHAMKEAW come from?
All FDA import refusal data for MANOP MEEKHAMKEAW 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.