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Amk Food Export (Pvt) Ltd.

⚠️ Moderate Risk

FEI: 3004027094 • Dehiwala, Colombo • SRI LANKA

FEI

FEI Number

3004027094

📍

Location

Dehiwala, Colombo

🇱🇰

Country

SRI LANKA
🏢

Address

146/7 Dutugamunu Street, , Dehiwala, Colombo, Sri Lanka

Moderate Risk

FDA Import Risk Assessment

46.3
LowModerateHighCritical

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

Statistics

14
Total Refusals
10
Unique Violations
3/20/2010
Latest Refusal
10/25/2005
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
31.8×10%
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

2497×

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.

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.

2812×

BACTERIA

The article appears to contain a poisonous and deleterious substance which may render it injurious to health. Contains

3082×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

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).

2181×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

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.

2511×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

3211×

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.

Refusal History

DateProductViolationsDivision
3/20/2010
16YCT99FISHERY PRODUCTS, N.E.C.
249FILTHY
Los Angeles District Office (LOS-DO)
7/27/2009
36AGT03CANE SUGAR (SUCROSE)
249FILTHY
308MFR INSAN
Los Angeles District Office (LOS-DO)
7/27/2009
36AGT03CANE SUGAR (SUCROSE)
249FILTHY
308MFR INSAN
Los Angeles District Office (LOS-DO)
2/12/2009
16AGF99FISH, N.E.C.
249FILTHY
Los Angeles District Office (LOS-DO)
8/9/2007
16AMT42SWORDFISH
251POISONOUS
Los Angeles District Office (LOS-DO)
2/6/2007
04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C.
274COLOR LBLG
321LACKS N/C
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
12/28/2006
16YVT99FISHERY PRODUCTS, N.E.C.
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
12/28/2006
16YVT99FISHERY PRODUCTS, N.E.C.
249FILTHY
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
12/28/2006
16YVT99FISHERY PRODUCTS, N.E.C.
249FILTHY
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
12/28/2006
16YVT99FISHERY PRODUCTS, N.E.C.
249FILTHY
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
7/6/2006
16AVE99FISH, N.E.C.
281BACTERIA
Los Angeles District Office (LOS-DO)
7/6/2006
16AVE99FISH, N.E.C.
281BACTERIA
Los Angeles District Office (LOS-DO)
5/2/2006
25LCE25ONION BULB (YELLOW, WHITE, RED, ETC.), DRIED OR PASTE
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
10/25/2005
16YGT99FISHERY PRODUCTS, N.E.C.
218LIST INGRE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Amk Food Export (Pvt) Ltd.'s FDA import refusal history?

Amk Food Export (Pvt) Ltd. (FEI: 3004027094) has 14 FDA import refusal record(s) in our database, spanning from 10/25/2005 to 3/20/2010.

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 Food Export (Pvt) Ltd.'s FEI number is 3004027094.

What types of violations has Amk Food Export (Pvt) Ltd. received?

Amk Food Export (Pvt) Ltd. has been cited for 10 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 Food Export (Pvt) Ltd. come from?

All FDA import refusal data for Amk Food Export (Pvt) Ltd. 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.