ImportRefusal LogoImportRefusal

Al Harmoodi Computer Systems

⚠️ Moderate Risk

FEI: 3005742067 • Dubai • UNITED ARAB EMIRATES

FEI

FEI Number

3005742067

📍

Location

Dubai

🇦🇪
🏢

Address

Murshed Bazar, , Dubai, , United Arab Emirates

Moderate Risk

FDA Import Risk Assessment

44.8
LowModerateHighCritical

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

Statistics

41
Total Refusals
16
Unique Violations
12/31/2015
Latest Refusal
6/27/2008
Earliest Refusal

Score Breakdown

Violation Severity
53.2×40%
Refusal Volume
60.1×30%
Recency
0.0×20%
Frequency
54.6×10%
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

47117×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

47510×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

759×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

1976×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

1186×

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).

4733×

LABELING

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

2183×

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.

3332×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

3202×

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.

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).

3352×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

4742×

COSMETLBLG

It appears the label does not bear the common or usual name of the cosmetic.

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2351×

NOT IMPACT

The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.

4831×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

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.

Refusal History

DateProductViolationsDivision
12/31/2015
50NGY18HENNA
11UNSAFE COL
Detroit District Office (DET-DO)
12/2/2015
53DD02PERFUMES (FRAGRANCE PREPARATIONS)
471CSTIC LBLG
474COSMETLBLG
475COSMETLBLG
New Orleans District Office (NOL-DO)
8/26/2015
55QP16GLYCERIN (PHARMACEUTIC NECESSITY - HUMECTANT)
118NOT LISTED
333LACKS FIRM
335LACKS N/C
75UNAPPROVED
New Orleans District Office (NOL-DO)
1/13/2015
63VDL02HYDROQUINONE (DEPIGMENTOR)
16DIRECTIONS
75UNAPPROVED
New Orleans District Office (NOL-DO)
11/26/2014
53CD02EYELINER (EYE MAKEUP PREPARATIONS)
197COSM COLOR
471CSTIC LBLG
474COSMETLBLG
475COSMETLBLG
New Orleans District Office (NOL-DO)
6/18/2014
53DD02PERFUMES (FRAGRANCE PREPARATIONS)
471CSTIC LBLG
475COSMETLBLG
New Orleans District Office (NOL-DO)
4/4/2014
31KGT99TEA, N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
New Orleans District Office (NOL-DO)
4/4/2014
53CH03EYE SHADOW (EYE MAKEUP PREPARATIONS)
197COSM COLOR
471CSTIC LBLG
New Orleans District Office (NOL-DO)
6/21/2013
53DD02PERFUMES (FRAGRANCE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
5/16/2013
53CG99OTHER EYE MAKEUP PREPARATIONS, N.E.C.
197COSM COLOR
471CSTIC LBLG
New Orleans District Office (NOL-DO)
5/16/2013
53CG02EYELINER (EYE MAKEUP PREPARATIONS)
197COSM COLOR
New Orleans District Office (NOL-DO)
1/23/2013
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
New Orleans District Office (NOL-DO)
9/7/2012
53YD99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
197COSM COLOR
New Orleans District Office (NOL-DO)
8/17/2012
54FYT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
320LACKS FIRM
473LABELING
New Orleans District Office (NOL-DO)
8/17/2012
31GGT01COFFEE DRINK
218LIST INGRE
New Orleans District Office (NOL-DO)
8/17/2012
86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
118NOT LISTED
235NOT IMPACT
New Orleans District Office (NOL-DO)
8/14/2012
53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
8/14/2012
53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
8/14/2012
53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
8/10/2012
66VAL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
333LACKS FIRM
335LACKS N/C
473LABELING
New Orleans District Office (NOL-DO)
8/9/2012
53RC03EYE MAKE UP PREPARATIONS, COSMETIC PRODUCTS CONTAINING ANIMAL BY-PRODUCTS (BOVINE)
475COSMETLBLG
New Orleans District Office (NOL-DO)
8/9/2012
64XBJ06SALICYLIC ACID (KERATOLYTIC)
118NOT LISTED
75UNAPPROVED
New Orleans District Office (NOL-DO)
8/9/2012
50NGY18HENNA
11UNSAFE COL
New Orleans District Office (NOL-DO)
8/7/2012
65PDQ99REGULATOR N.E.C.
483DRUG NAME
75UNAPPROVED
New Orleans District Office (NOL-DO)
8/7/2012
53DD02PERFUMES (FRAGRANCE PREPARATIONS)
475COSMETLBLG
New Orleans District Office (NOL-DO)
8/7/2012
65PDY99REGULATOR N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
8/3/2012
53DD02PERFUMES (FRAGRANCE PREPARATIONS)
475COSMETLBLG
New Orleans District Office (NOL-DO)
7/31/2012
62GBX99ANTI-INFLAMMATORY N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
7/31/2012
53DD02PERFUMES (FRAGRANCE PREPARATIONS)
75UNAPPROVED
New Orleans District Office (NOL-DO)
6/7/2012
53LC06MOISTURIZING (SKIN CARE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
6/7/2012
53LC06MOISTURIZING (SKIN CARE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
6/7/2012
53LC06MOISTURIZING (SKIN CARE PREPARATIONS)
197COSM COLOR
471CSTIC LBLG
New Orleans District Office (NOL-DO)
5/11/2012
53PY99OTHER COSMETIC RAW MATERIALS, N.E.C.
471CSTIC LBLG
473LABELING
New Orleans District Office (NOL-DO)
12/12/2011
53LC99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
New Orleans District Office (NOL-DO)
12/12/2011
53LC99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
New Orleans District Office (NOL-DO)
12/12/2011
53DD02PERFUMES (FRAGRANCE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
12/12/2011
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
New Orleans District Office (NOL-DO)
8/5/2011
53JK01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
471CSTIC LBLG
475COSMETLBLG
New Orleans District Office (NOL-DO)
6/27/2008
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
475COSMETLBLG
New Orleans District Office (NOL-DO)
6/27/2008
53LC99OTHER SKIN CARE PREPARATIONS, N.E.C.
475COSMETLBLG
New Orleans District Office (NOL-DO)
6/27/2008
53LC99OTHER SKIN CARE PREPARATIONS, N.E.C.
475COSMETLBLG
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Al Harmoodi Computer Systems's FDA import refusal history?

Al Harmoodi Computer Systems (FEI: 3005742067) has 41 FDA import refusal record(s) in our database, spanning from 6/27/2008 to 12/31/2015.

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. Al Harmoodi Computer Systems's FEI number is 3005742067.

What types of violations has Al Harmoodi Computer Systems received?

Al Harmoodi Computer Systems has been cited for 16 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 Al Harmoodi Computer Systems come from?

All FDA import refusal data for Al Harmoodi Computer Systems 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.