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Macat Group New Advanced Technology Co. Ltd

⚠️ Moderate Risk

FEI: 3003852451 • Huizhou, Guangdong • CHINA

FEI

FEI Number

3003852451

📍

Location

Huizhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Macat Building F 10, NO 63 Liantangao Maidilu; Huicheng, Huizhou, Guangdong, China

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
12
Unique Violations
8/21/2007
Latest Refusal
1/30/2004
Earliest Refusal

Score Breakdown

Violation Severity
73.2×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
39.3×10%
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

2496×

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.

113×

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).

2451×

EXCESS SUL

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

2561×

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)).

2601×

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.

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.

3411×

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).

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

4821×

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.

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).

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.

1181×

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

DateProductViolationsDivision
8/21/2007
76EFWTOOTHBRUSH, MANUAL
118NOT LISTED
341REGISTERED
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
62NEEDS FCE
83NO PROCESS
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.
256INCONSPICU
260FALSE
San Francisco District Office (SAN-DO)
7/7/2004
33EGT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
11UNSAFE COL
321LACKS N/C
482NUTRIT LBL
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.