Amk Exporters
⚠️ Moderate Risk
FEI: 3005063804 • Colombo • SRI LANKA
FEI Number
3005063804
Location
Colombo
Country
SRI LANKAAddress
Unknown Street, , Colombo, , Sri Lanka
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
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.
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
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.
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/22/2009 | 02DVT01RICE, BROWN, PROCESSED (PACKAGED) | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 20RCE01APPLE, JAM, JELLY, PRESERVES, MARMALADE, BUTTER AND CANDIED | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 16ACE56FILEFISH | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 16ACE56FILEFISH | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 16ACE56FILEFISH | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 16ACE56FILEFISH | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 16ACE56FILEFISH | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 16ACE56FILEFISH | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 16ACE56FILEFISH | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 16ACE56FILEFISH | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 28JCE99MIXED SPICES AND SEASONING WITH SALT, N.E.C. | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 28JCE99MIXED SPICES AND SEASONING WITH SALT, N.E.C. | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 28JCE99MIXED SPICES AND SEASONING WITH SALT, N.E.C. | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 28JCE99MIXED SPICES AND SEASONING WITH SALT, N.E.C. | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 16ACE56FILEFISH | Baltimore District Office (BLT-DO) | |
| 8/7/2008 | 28JCE99MIXED SPICES AND SEASONING WITH SALT, N.E.C. | Baltimore District Office (BLT-DO) |
Frequently Asked Questions
What is Amk Exporters's FDA import refusal history?
Amk Exporters (FEI: 3005063804) has 16 FDA import refusal record(s) in our database, spanning from 8/7/2008 to 9/22/2009.
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. Amk Exporters's FEI number is 3005063804.
What types of violations has Amk Exporters received?
Amk Exporters has been cited for 5 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 Amk Exporters come from?
All FDA import refusal data for Amk Exporters 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.