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Beeden Internation

⚠️ High Risk

FEI: 3004445737 • Mumbai • INDIA

FEI

FEI Number

3004445737

📍

Location

Mumbai

🇮🇳

Country

INDIA
🏢

Address

Shop No D 3-88 Mi, , Mumbai, , India

High Risk

FDA Import Risk Assessment

52.9
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

11
Total Refusals
5
Unique Violations
4/13/2004
Latest Refusal
4/12/2004
Earliest Refusal

Score Breakdown

Violation Severity
77.3×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
100.0×10%
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

757×

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).

1781×

COL ADDED

The article appears to bear or contain, for the purpose of coloring only, a color additive which is unsafe within the meaning of Section 721(a).

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

3311×

DR QUALITC

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the drug appears to be represented as not being recognized in an official compendium and appears its strength differs from or its quality or purity falls below, that which it purports or is represented to possess.

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

Refusal History

DateProductViolationsDivision
4/13/2004
65LBJ99PROTECTANT N.E.C.
336INCONSPICU
New Orleans District Office (NOL-DO)
4/12/2004
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
331DR QUALITC
New Orleans District Office (NOL-DO)
4/12/2004
28YGH99SPICES, FLAVORS AND SALT NOT MENTIONED ELSEWHERE, N.E.C.
328USUAL NAME
New Orleans District Office (NOL-DO)
4/12/2004
61PAA99ANTI-DIABETIC N.E.C.
178COL ADDED
New Orleans District Office (NOL-DO)
4/12/2004
54ABA90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN)
75UNAPPROVED
New Orleans District Office (NOL-DO)
4/12/2004
62UAH99ANTI-TUSSIVE/COLD N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
4/12/2004
62UAH99ANTI-TUSSIVE/COLD N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
4/12/2004
62UAH99ANTI-TUSSIVE/COLD N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
4/12/2004
62CAA99ANTI-HYPERTENSIVE N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
4/12/2004
61PAA99ANTI-DIABETIC N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
4/12/2004
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Beeden Internation's FDA import refusal history?

Beeden Internation (FEI: 3004445737) has 11 FDA import refusal record(s) in our database, spanning from 4/12/2004 to 4/13/2004.

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. Beeden Internation's FEI number is 3004445737.

What types of violations has Beeden Internation received?

Beeden Internation has been cited for 5 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 Beeden Internation come from?

All FDA import refusal data for Beeden Internation 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.