Macat Group New Advanced Technology Co. Ltd
⚠️ Moderate Risk
FEI: 3003852451 • Huizhou, Guangdong • CHINA
FEI Number
3003852451
Location
Huizhou, Guangdong
Country
CHINAAddress
Macat Building F 10, NO 63 Liantangao Maidilu; Huicheng, Huizhou, Guangdong, China
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
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.
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).
EXCESS SUL
The article appears to contain excessive sulfites, a poisonous and deleterious substance which may render it injurious to health.
INCONSPICU
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
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.
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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).
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.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/21/2007 | 76EFWTOOTHBRUSH, MANUAL | New York District Office (NYK-DO) | |
| 4/19/2007 | 25JGH24GINGER ROOT (ROOT & TUBER VEGETABLE) | 11UNSAFE COL | New York District Office (NYK-DO) |
| 12/6/2006 | 25JGH24GINGER ROOT (ROOT & TUBER VEGETABLE) | 245EXCESS SUL | New York District Office (NYK-DO) |
| 11/1/2005 | 25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C. | 249FILTHY | New York District Office (NYK-DO) |
| 9/14/2005 | 21GGH05DATES (PIT FRUIT), (PIT FRUIT) | 11UNSAFE COL | New York District Office (NYK-DO) |
| 4/29/2005 | 21GGH05DATES (PIT FRUIT), (PIT FRUIT) | 249FILTHY | New York District Office (NYK-DO) |
| 10/20/2004 | 37JCT17BEAN, GROUND SAUCE | New York District Office (NYK-DO) | |
| 7/8/2004 | 04YGT04RICE STICKS | 249FILTHY | San Francisco District Office (SAN-DO) |
| 7/8/2004 | 04YGT04RICE STICKS | 249FILTHY | San Francisco District Office (SAN-DO) |
| 7/8/2004 | 04YGT04RICE STICKS | 249FILTHY | San Francisco District Office (SAN-DO) |
| 7/8/2004 | 04YGT04RICE STICKS | 249FILTHY | San Francisco District Office (SAN-DO) |
| 7/7/2004 | 54FAY99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | San Francisco District Office (SAN-DO) | |
| 7/7/2004 | 33EGT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE) | San Francisco District Office (SAN-DO) | |
| 1/30/2004 | 31PGT99TEA SUBSTITUTES, N.E.C. | 473LABELING | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Macat Group New Advanced Technology Co. Ltd's FDA import refusal history?
Macat Group New Advanced Technology Co. Ltd (FEI: 3003852451) has 14 FDA import refusal record(s) in our database, spanning from 1/30/2004 to 8/21/2007.
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. Macat Group New Advanced Technology Co. Ltd's FEI number is 3003852451.
What types of violations has Macat Group New Advanced Technology Co. Ltd received?
Macat Group New Advanced Technology Co. Ltd has been cited for 12 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 Macat Group New Advanced Technology Co. Ltd come from?
All FDA import refusal data for Macat Group New Advanced Technology 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.