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FIDAI TRADING ENTERPRISE

⚠️ Moderate Risk

FEI: 3004249920 • Karachi, Sindh • PAKISTAN

FEI

FEI Number

3004249920

📍

Location

Karachi, Sindh

🇵🇰

Country

PAKISTAN
🏢

Address

8/3 Arkay Square Extension, New Challi, Karachi, Sindh, Pakistan

Moderate Risk

FDA Import Risk Assessment

44.6
LowModerateHighCritical

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

Statistics

15
Total Refusals
13
Unique Violations
10/19/2010
Latest Refusal
5/21/2004
Earliest Refusal

Score Breakdown

Violation Severity
72.1×40%
Refusal Volume
44.6×30%
Recency
0.0×20%
Frequency
23.4×10%
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

115×

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).

755×

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).

162×

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.

1972×

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).

832×

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.

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).

3212×

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.

4732×

LABELING

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

642×

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.

2491×

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.

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

2761×

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.

1171×

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

DateProductViolationsDivision
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)
473LABELING
83NO PROCESS
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.
117DANGEROUS
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
9/19/2005
62UAY99ANTI-TUSSIVE/COLD N.E.C.
118NOT LISTED
75UNAPPROVED
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.
11UNSAFE COL
321LACKS N/C
64YELLOW #5
San Francisco District Office (SAN-DO)
6/27/2005
13BHT99CUSTARD, N.E.C.
11UNSAFE COL
321LACKS N/C
64YELLOW #5
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.
11UNSAFE COL
274COLOR LBLG
276PRESRV LBL
473LABELING
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.
16DIRECTIONS
75UNAPPROVED
Southwest Import District Office (SWI-DO)
5/21/2004
60SBA99ANTACID, N.E.C.
16DIRECTIONS
75UNAPPROVED
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.