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Intimex Hochiminh

⚠️ Moderate Risk

FEI: 3004270695 • Hochiminh City, Vn-65 • VIETNAM

FEI

FEI Number

3004270695

📍

Location

Hochiminh City, Vn-65

🇻🇳

Country

VIETNAM
🏢

Address

1, 61nguyenvangiai, Dakao Ward, District, , Hochiminh City, Vn-65, Vietnam

Moderate Risk

FDA Import Risk Assessment

48.0
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

18
Total Refusals
13
Unique Violations
1/18/2007
Latest Refusal
3/14/2003
Earliest Refusal

Score Breakdown

Violation Severity
72.9×40%
Refusal Volume
47.4×30%
Recency
0.0×20%
Frequency
46.7×10%
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

629×

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).

838×

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.

2492×

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.

112×

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).

2182×

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.

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

3201×

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.

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.

3241×

NO ENGLISH

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)).

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.

2451×

EXCESS SUL

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

641×

YELLOW #5

The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.

20401×

SULFITELBL

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.

Refusal History

DateProductViolationsDivision
1/18/2007
31AYB01COFFEE, BEANS
249FILTHY
New Orleans District Office (NOL-DO)
12/11/2006
54EYY99HERBALS & BOTANICAL TEAS, N.E.C.
218LIST INGRE
324NO ENGLISH
482NUTRIT LBL
Baltimore District Office (BLT-DO)
12/11/2006
02DGT09RICE, JASMINE, PROCESSED (PACKAGED)
218LIST INGRE
320LACKS FIRM
321LACKS N/C
Baltimore District Office (BLT-DO)
9/13/2006
16YCT12SHRIMP PASTE, FISHERY PRODUCTS, N.E.C.
11UNSAFE COL
Baltimore District Office (BLT-DO)
7/25/2006
24FCT01EGG PLANT (FRUIT USED AS VEGETABLE)
83NO PROCESS
New York District Office (NYK-DO)
7/25/2006
24FCT01EGG PLANT (FRUIT USED AS VEGETABLE)
83NO PROCESS
New York District Office (NYK-DO)
7/25/2006
25JCT21GARLIC BULB (ROOT & TUBER VEGETABLE)
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
6/26/2006
25JCT18LOTUS ROOT (ROOT & TUBER VEGETABLE)
2040SULFITELBL
245EXCESS SUL
Los Angeles District Office (LOS-DO)
6/26/2006
33LHT06FLAVORED CANDY, SOFT (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
249FILTHY
308MFR INSAN
Los Angeles District Office (LOS-DO)
6/26/2006
33LCT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
6/26/2006
33LHT06FLAVORED CANDY, SOFT (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
64YELLOW #5
Los Angeles District Office (LOS-DO)
3/14/2006
16YCE12SHRIMP PASTE, FISHERY PRODUCTS, N.E.C.
62NEEDS FCE
Los Angeles District Office (LOS-DO)
3/14/2006
16YCE12SHRIMP PASTE, FISHERY PRODUCTS, N.E.C.
62NEEDS FCE
Los Angeles District Office (LOS-DO)
3/14/2006
16YCE12SHRIMP PASTE, FISHERY PRODUCTS, N.E.C.
62NEEDS FCE
Los Angeles District Office (LOS-DO)
3/14/2003
37JCE05SOY SAUCE
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
3/14/2003
16ACT73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22')
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
3/14/2003
24VCT99LEAF & STEM VEGETABLES, WITH SAUCE, N.E.C.
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
3/14/2003
16YCE12SHRIMP PASTE, FISHERY PRODUCTS, N.E.C.
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Intimex Hochiminh's FDA import refusal history?

Intimex Hochiminh (FEI: 3004270695) has 18 FDA import refusal record(s) in our database, spanning from 3/14/2003 to 1/18/2007.

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. Intimex Hochiminh's FEI number is 3004270695.

What types of violations has Intimex Hochiminh received?

Intimex Hochiminh has been cited for 13 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 Intimex Hochiminh come from?

All FDA import refusal data for Intimex Hochiminh 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.