C&A Products Co., Ltd.
⚠️ Moderate Risk
FEI: 3002975267 • Ratchaburi, TH-70 • THAILAND
FEI Number
3002975267
Location
Ratchaburi, TH-70
Country
THAILANDAddress
222 Moo 3, Tumbol Pongswai, Ratchaburi, TH-70, 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
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.
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.
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.
NONRSP-VER
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to have been prepared or packed under insanitary conditions whereby it may have been rendered injurious to health due to inadequate processing in that the scheduled process filed by the manufacturer for this thermally processed low acid food packaged in a hermetically sealed container pursuant to 21 CFR 108.35 (c)(2) appears to be inadequate to protect the public health.
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.
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 |
|---|---|---|---|
| 4/14/2005 | 30YEE02COCONUT MILK BEVERAGE BASE | 3160NONRSP-VER | New York District Office (NYK-DO) |
| 11/2/2004 | 22KEY99OTHER FRUITS AND FRUIT PRODUCTS, OTHER FRUIT JUICES OR CONCENTRATES, N.E.C. | 83NO PROCESS | Florida District Office (FLA-DO) |
| 10/13/2004 | 30YEE02COCONUT MILK BEVERAGE BASE | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 10/13/2004 | 29AEE99NONCARBONATED SOFT DRINK, N.E.C. | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 10/13/2004 | 29AEE99NONCARBONATED SOFT DRINK, N.E.C. | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 8/3/2004 | 21XET14TAMARIND (SUBTROPICAL/TROPICAL FRUIT PULP) | 249FILTHY | San Francisco District Office (SAN-DO) |
| 2/6/2004 | 30YEE02COCONUT MILK BEVERAGE BASE | 83NO PROCESS | Baltimore District Office (BLT-DO) |
| 12/17/2003 | 29AEE99NONCARBONATED SOFT DRINK, N.E.C. | 83NO PROCESS | Baltimore District Office (BLT-DO) |
| 8/21/2003 | 28CEP99NATURAL EXTRACT OR FLAVOR, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 7/22/2003 | 21SET99SUBTROPICAL AND TROPICAL FRUIT, N.E.C. | New York District Office (NYK-DO) | |
| 6/5/2003 | 29BEE99CARBONATED SOFT DRINK, N.E.C. | 83NO PROCESS | New York District Office (NYK-DO) |
| 6/5/2003 | 29BEE99CARBONATED SOFT DRINK, N.E.C. | 83NO PROCESS | New York District Office (NYK-DO) |
Frequently Asked Questions
What is C&A Products Co., Ltd.'s FDA import refusal history?
C&A Products Co., Ltd. (FEI: 3002975267) has 12 FDA import refusal record(s) in our database, spanning from 6/5/2003 to 4/14/2005.
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. C&A Products Co., Ltd.'s FEI number is 3002975267.
What types of violations has C&A Products Co., Ltd. received?
C&A Products 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 C&A Products Co., Ltd. come from?
All FDA import refusal data for C&A Products 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.