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Dovetee Nigeria

⚠️ Moderate Risk

FEI: 3005065677 • Lekki, Lagos State • NIGERIA

FEI

FEI Number

3005065677

📍

Location

Lekki, Lagos State

🇳🇬

Country

NIGERIA
🏢

Address

Km 22, Lagos-Epe Expressway, Olokonla, Lekki, Lagos State, Nigeria

Moderate Risk

FDA Import Risk Assessment

30.7
LowModerateHighCritical

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

Statistics

14
Total Refusals
12
Unique Violations
4/9/2013
Latest Refusal
8/28/2006
Earliest Refusal

Score Breakdown

Violation Severity
38.7×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
21.1×10%
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

32810×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

32110×

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.

3208×

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.

2188×

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.

1182×

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).

4712×

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.

4752×

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.

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.

3351×

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.

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.

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.

2511×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

Refusal History

DateProductViolationsDivision
4/9/2013
41YAH99DIETARY CONVENTIONAL FOODS, N.E.C.
218LIST INGRE
251POISONOUS
321LACKS N/C
328USUAL NAME
Southwest Import District Office (SWI-DO)
1/30/2009
02GYH99FLOURS AND MEALS N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
New Orleans District Office (NOL-DO)
1/30/2009
25YYB99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
New Orleans District Office (NOL-DO)
1/30/2009
02GYH99FLOURS AND MEALS N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
New Orleans District Office (NOL-DO)
1/26/2009
28YYY99SPICES, FLAVORS AND SALT NOT MENTIONED ELSEWHERE, N.E.C.
260FALSE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
New Orleans District Office (NOL-DO)
1/23/2009
53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
471CSTIC LBLG
475COSMETLBLG
New Orleans District Office (NOL-DO)
1/23/2009
53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
471CSTIC LBLG
475COSMETLBLG
New Orleans District Office (NOL-DO)
1/23/2009
28MFE99IMITATION FLAVOR, N.E.C.
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
New Orleans District Office (NOL-DO)
1/23/2009
28FYY99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
New Orleans District Office (NOL-DO)
1/23/2009
28FYY99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
New Orleans District Office (NOL-DO)
1/23/2009
25YYB99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
New Orleans District Office (NOL-DO)
1/23/2009
02GYH99FLOURS AND MEALS N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
New Orleans District Office (NOL-DO)
1/23/2009
53YH99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
118NOT LISTED
New Orleans District Office (NOL-DO)
8/28/2006
62FBY99ANTI-INFECTIVE, TOPICAL N.E.C.
118NOT LISTED
16DIRECTIONS
335LACKS N/C
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Dovetee Nigeria's FDA import refusal history?

Dovetee Nigeria (FEI: 3005065677) has 14 FDA import refusal record(s) in our database, spanning from 8/28/2006 to 4/9/2013.

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. Dovetee Nigeria's FEI number is 3005065677.

What types of violations has Dovetee Nigeria received?

Dovetee Nigeria 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 Dovetee Nigeria come from?

All FDA import refusal data for Dovetee Nigeria 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.