FIDAI TRADING ENTERPRISE
⚠️ Moderate Risk
FEI: 3004249920 • Karachi, Sindh • PAKISTAN
FEI Number
3004249920
Location
Karachi, Sindh
Country
PAKISTANAddress
8/3 Arkay Square Extension, New Challi, Karachi, Sindh, 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
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).
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.
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).
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.
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).
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
PRESRV LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.
DANGEROUS
The article appears to be dangerous to health when used in the dosage or manner, or with the frequency or duration, prescribed, recommended, or suggested in the labeling thereof.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/19/2010 | 53FH06HAIR LIGHTENERS, WITH COLOR (HAIR COLORING PREPARATIONS) | 197COSM COLOR | New York District Office (NYK-DO) |
| 9/29/2010 | 35AGT01GELATIN, FLAVORED | 11UNSAFE COL | San Francisco District Office (SAN-DO) |
| 4/5/2010 | 27YCE99CONDIMENTS, N.E.C. | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 4/28/2009 | 25JHP21GARLIC BULB (ROOT & TUBER VEGETABLE) | San Francisco District Office (SAN-DO) | |
| 4/16/2009 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | San Francisco District Office (SAN-DO) |
| 11/17/2005 | 66VCL99MISCELLANEOUS PATENT MEDICINES, ETC. | San Francisco District Office (SAN-DO) | |
| 9/19/2005 | 62UAY99ANTI-TUSSIVE/COLD N.E.C. | San Francisco District Office (SAN-DO) | |
| 8/13/2005 | 21HGH05DATES, DRIED OR PASTE | 249FILTHY | New York District Office (NYK-DO) |
| 6/27/2005 | 13BHT99CUSTARD, N.E.C. | San Francisco District Office (SAN-DO) | |
| 6/27/2005 | 13BHT99CUSTARD, N.E.C. | San Francisco District Office (SAN-DO) | |
| 6/27/2005 | 13BHT99CUSTARD, N.E.C. | 11UNSAFE COL | San Francisco District Office (SAN-DO) |
| 6/16/2004 | 37JHE99SAUCES, N.E.C. | Southwest Import District Office (SWI-DO) | |
| 5/21/2004 | 53GD04LEG AND BODY PAINTS (MAKEUP PREPARATIONS, NOT FOR EYES) | 197COSM COLOR | Southwest Import District Office (SWI-DO) |
| 5/21/2004 | 66VBO99MISCELLANEOUS PATENT MEDICINES, ETC. | Southwest Import District Office (SWI-DO) | |
| 5/21/2004 | 60SBA99ANTACID, N.E.C. | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is FIDAI TRADING ENTERPRISE's FDA import refusal history?
FIDAI TRADING ENTERPRISE (FEI: 3004249920) has 15 FDA import refusal record(s) in our database, spanning from 5/21/2004 to 10/19/2010.
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. FIDAI TRADING ENTERPRISE's FEI number is 3004249920.
What types of violations has FIDAI TRADING ENTERPRISE received?
FIDAI TRADING ENTERPRISE 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 FIDAI TRADING ENTERPRISE come from?
All FDA import refusal data for FIDAI TRADING ENTERPRISE 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.