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Marhaba Laboratories Pvt Ltd

⚠️ Moderate Risk

FEI: 3010006690 • Lahore • PAKISTAN

FEI

FEI Number

3010006690

📍

Location

Lahore

🇵🇰

Country

PAKISTAN
🏢

Address

142-Quaid E Azam Industrial Estate, , Lahore, , Pakistan

Moderate Risk

FDA Import Risk Assessment

40.1
LowModerateHighCritical

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

Statistics

15
Total Refusals
8
Unique Violations
7/31/2013
Latest Refusal
5/14/2009
Earliest Refusal

Score Breakdown

Violation Severity
57.9×40%
Refusal Volume
44.6×30%
Recency
0.0×20%
Frequency
35.6×10%
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

4886×

HEALTH C

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 bears an unauthorized nutrient content/health claim.

754×

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).

2563×

INCONSPICU

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

23002×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

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.

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.

1181×

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).

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.

Refusal History

DateProductViolationsDivision
7/31/2013
53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
16DIRECTIONS
New York District Office (NYK-DO)
5/13/2011
36CHT04HONEY
482NUTRIT LBL
New York District Office (NYK-DO)
4/18/2011
54IDT02PSYLLIUM (FIBER)
256INCONSPICU
260FALSE
New York District Office (NYK-DO)
4/18/2011
54IDT02PSYLLIUM (FIBER)
256INCONSPICU
New York District Office (NYK-DO)
4/18/2011
54IDT02PSYLLIUM (FIBER)
256INCONSPICU
New York District Office (NYK-DO)
3/24/2011
66VAL99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Seattle District Office (SEA-DO)
3/24/2011
66VAR99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Seattle District Office (SEA-DO)
3/24/2011
66VAR99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Seattle District Office (SEA-DO)
12/14/2010
31KFT99TEA, N.E.C.
488HEALTH C
Florida District Office (FLA-DO)
12/14/2010
31KFT99TEA, N.E.C.
488HEALTH C
Florida District Office (FLA-DO)
12/14/2010
02DCT99RICE, PROCESSED (PACKAGED) N.E.C.
488HEALTH C
Florida District Office (FLA-DO)
12/14/2010
02DCT99RICE, PROCESSED (PACKAGED) N.E.C.
488HEALTH C
Florida District Office (FLA-DO)
10/6/2010
66VAR99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
5/14/2009
54IDR99FIBER, N.E.C.
2300DIETARYLBL
488HEALTH C
Los Angeles District Office (LOS-DO)
5/14/2009
54IDR99FIBER, N.E.C.
2300DIETARYLBL
488HEALTH C
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Marhaba Laboratories Pvt Ltd's FDA import refusal history?

Marhaba Laboratories Pvt Ltd (FEI: 3010006690) has 15 FDA import refusal record(s) in our database, spanning from 5/14/2009 to 7/31/2013.

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. Marhaba Laboratories Pvt Ltd's FEI number is 3010006690.

What types of violations has Marhaba Laboratories Pvt Ltd received?

Marhaba Laboratories Pvt Ltd 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 Marhaba Laboratories Pvt Ltd come from?

All FDA import refusal data for Marhaba Laboratories Pvt Ltd 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.