Chotiwat Manufacturing Public Co., Ltd.
⚠️ Moderate Risk
FEI: 3004310173 • Hat Yai, Songkhla • THAILAND
FEI Number
3004310173
Location
Hat Yai, Songkhla
Country
THAILANDAddress
1069 ASIA HIGHWAY ROAD, Khohong Sub District, Hat Yai, Songkhla, 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.
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.
LACKS FIRM
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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
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.
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 |
|---|---|---|---|
| 11/13/2015 | 16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | New Orleans District Office (NOL-DO) |
| 1/30/2009 | 16YCE09FISH SAUCE, FISHERY PRODUCTS, N.E.C. | 83NO PROCESS | New York District Office (NYK-DO) |
| 5/7/2007 | 37JCT99SAUCES, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 9/15/2004 | 16IEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.), HOT SMOKED, FISH | 83NO PROCESS | Cincinnati District Office (CIN-DO) |
| 9/15/2004 | 16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 83NO PROCESS | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Chotiwat Manufacturing Public Co., Ltd.'s FDA import refusal history?
Chotiwat Manufacturing Public Co., Ltd. (FEI: 3004310173) has 5 FDA import refusal record(s) in our database, spanning from 9/15/2004 to 11/13/2015.
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. Chotiwat Manufacturing Public Co., Ltd.'s FEI number is 3004310173.
What types of violations has Chotiwat Manufacturing Public Co., Ltd. received?
Chotiwat Manufacturing Public Co., Ltd. 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 Chotiwat Manufacturing Public Co., Ltd. come from?
All FDA import refusal data for Chotiwat Manufacturing Public 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.