A.Q. & Company
⚠️ Moderate Risk
FEI: 3003333240 • Karachi • PAKISTAN
FEI Number
3003333240
Location
Karachi
Country
PAKISTANAddress
10-11 Eidgah M. A. Jinnah Roadg. P. O., , Karachi, , Pakistan
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
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).
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.
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.
COSMETFPLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an undeclared color additive which renders it misbranded within the meaning of Sections 1454(c)(3)(B) and 1456 of the Fair Packaging and Labeling Act.
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.
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).
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).
COLOR LBLG
The color additive appears to not have its packaging and labeling in conformity with such requirements as issued under section 721.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/13/2019 | 53CY01EYEBROW PENCIL (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Division of Northeast Imports (DNEI) |
| 8/19/2019 | 53CK02EYELINER (EYE MAKEUP PREPARATIONS) | Division of Northern Border Imports (DNBI) | |
| 2/15/2017 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | Division of Northeast Imports (DNEI) | |
| 6/8/2016 | 53CY99OTHER EYE MAKEUP PREPARATIONS, N.E.C. | 197COSM COLOR | Cincinnati District Office (CIN-DO) |
| 6/24/2015 | 53CY02EYELINER (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Cincinnati District Office (CIN-DO) |
| 11/26/2014 | 53CD02EYELINER (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | New Orleans District Office (NOL-DO) |
| 11/26/2014 | 53CD02EYELINER (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | New Orleans District Office (NOL-DO) |
| 8/22/2014 | 53CC08EYE MAKEUP KITS (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Minneapolis District Office (MIN-DO) |
| 11/22/2013 | 53CY02EYELINER (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Minneapolis District Office (MIN-DO) |
| 8/23/2012 | 53CY02EYELINER (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Chicago District Office (CHI-DO) |
| 7/27/2012 | 53CG02EYELINER (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | New Orleans District Office (NOL-DO) |
| 7/13/2012 | 53CD99OTHER EYE MAKEUP PREPARATIONS, N.E.C. | 471CSTIC LBLG | New Orleans District Office (NOL-DO) |
| 7/13/2012 | 53CD99OTHER EYE MAKEUP PREPARATIONS, N.E.C. | 197COSM COLOR | New Orleans District Office (NOL-DO) |
| 6/12/2012 | 53CC02EYELINER (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | New Orleans District Office (NOL-DO) |
| 6/1/2012 | 53CK02EYELINER (EYE MAKEUP PREPARATIONS) | San Francisco District Office (SAN-DO) | |
| 5/22/2012 | 53CK02EYELINER (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | New Orleans District Office (NOL-DO) |
| 11/4/2010 | 53CK02EYELINER (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Philadelphia District Office (PHI-DO) |
| 7/21/2009 | 53CY02EYELINER (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Detroit District Office (DET-DO) |
| 6/19/2009 | 53CK02EYELINER (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Southwest Import District Office (SWI-DO) |
| 3/17/2004 | 53CY02EYELINER (EYE MAKEUP PREPARATIONS) | 11UNSAFE COL | Minneapolis District Office (MIN-DO) |
Frequently Asked Questions
What is A.Q. & Company's FDA import refusal history?
A.Q. & Company (FEI: 3003333240) has 20 FDA import refusal record(s) in our database, spanning from 3/17/2004 to 11/13/2019.
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. A.Q. & Company's FEI number is 3003333240.
What types of violations has A.Q. & Company received?
A.Q. & Company has been cited for 8 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 A.Q. & Company come from?
All FDA import refusal data for A.Q. & Company 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.