Lane Chung Co Ltd
⚠️ Moderate Risk
FEI: 3002541753 • Hsien • TAIWAN
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
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).
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).
CYCLAMATE
The article appears to bear or contain cyclamate, an unsafe food additive within the meaning of Section 409
SACCHARLBL
The article contains Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient
DULCIN
The article appears to bear or contain dulcin, an unsafe food additive within the meaning of Section 409
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/22/2009 | 29CEE99NONALCOHOLIC BEVERAGES, N.E.C. | New York District Office (NYK-DO) | |
| 5/12/2009 | 21GGI14PLUM (PIT FRUIT) | New York District Office (NYK-DO) | |
| 5/12/2009 | 21GGI14PLUM (PIT FRUIT) | New York District Office (NYK-DO) | |
| 5/12/2009 | 21SGI04GUAVA (SUBTROPICAL AND TROPICAL FRUIT) | New York District Office (NYK-DO) | |
| 5/12/2009 | 21SGI05MANGO (SUBTROPICAL AND TROPICAL FRUIT) | New York District Office (NYK-DO) | |
| 5/12/2009 | 20NGI03PEAR (CORE FRUIT) | New York District Office (NYK-DO) | |
| 5/12/2009 | 21GGI14PLUM (PIT FRUIT) | New York District Office (NYK-DO) | |
| 7/28/2005 | 25PEE03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI) | 62NEEDS FCE | New York District Office (NYK-DO) |
| 7/28/2005 | 16EEE03OYSTERS | 62NEEDS FCE | New York District Office (NYK-DO) |
| 7/28/2005 | 25PEE03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI) | 62NEEDS FCE | New York District Office (NYK-DO) |
| 7/28/2005 | 29CEE99NONALCOHOLIC BEVERAGES, N.E.C. | 62NEEDS FCE | New York District Office (NYK-DO) |
| 7/28/2005 | 24CEE99BEAN, CORN, PEA WITH SAUCE, N.E.C. (VEGETABLE) | 62NEEDS FCE | New York District Office (NYK-DO) |
| 7/28/2005 | 24CEE99BEAN, CORN, PEA WITH SAUCE, N.E.C. (VEGETABLE) | 62NEEDS FCE | New York District Office (NYK-DO) |
| 7/28/2005 | 24AEE07KIDNEY BEAN | 62NEEDS FCE | New York District Office (NYK-DO) |
| 7/28/2005 | 30YEE02COCONUT MILK BEVERAGE BASE | 62NEEDS FCE | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Lane Chung Co Ltd's FDA import refusal history?
Lane Chung Co Ltd (FEI: 3002541753) has 15 FDA import refusal record(s) in our database, spanning from 7/28/2005 to 7/22/2009.
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. Lane Chung Co Ltd's FEI number is 3002541753.
What types of violations has Lane Chung Co Ltd received?
Lane Chung Co Ltd has been cited for 6 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 Lane Chung Co Ltd come from?
All FDA import refusal data for Lane Chung Co 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.