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B.P Industries (Pvt) Ltd

✅ Low Risk

FEI: 3004958662 • Karachi, Sindh • PAKISTAN

FEI

FEI Number

3004958662

📍

Location

Karachi, Sindh

🇵🇰

Country

PAKISTAN
🏢

Address

A-30 S.I.T.E, , Karachi, Sindh, Pakistan

Low Risk

FDA Import Risk Assessment

23.7
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
6
Unique Violations
6/13/2002
Latest Refusal
6/13/2002
Earliest Refusal

Score Breakdown

Violation Severity
48.3×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

111×

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).

2181×

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.

3201×

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.

3211×

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.

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.

641×

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.

Refusal History

DateProductViolationsDivision
6/13/2002
34ADT99COCOA BEAN N.E.C.
11UNSAFE COL
218LIST INGRE
320LACKS FIRM
321LACKS N/C
482NUTRIT LBL
64YELLOW #5
Detroit District Office (DET-DO)

Frequently Asked Questions

What is B.P Industries (Pvt) Ltd's FDA import refusal history?

B.P Industries (Pvt) Ltd (FEI: 3004958662) has 1 FDA import refusal record(s) in our database, spanning from 6/13/2002 to 6/13/2002.

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. B.P Industries (Pvt) Ltd's FEI number is 3004958662.

What types of violations has B.P Industries (Pvt) Ltd received?

B.P Industries (Pvt) Ltd has been cited for 6 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 B.P Industries (Pvt) Ltd come from?

All FDA import refusal data for B.P Industries (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.