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SHREE JAYAKALI JADIBUTI UDHYOG P

⚠️ Moderate Risk

FEI: 3013360537 • Kathmandu, Kathmandu • NEPAL

FEI

FEI Number

3013360537

📍

Location

Kathmandu, Kathmandu

🇳🇵

Country

NEPAL
🏢

Address

Balaju-16, , Kathmandu, Kathmandu, Nepal

Moderate Risk

FDA Import Risk Assessment

48.9
LowModerateHighCritical

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

Statistics

4
Total Refusals
6
Unique Violations
1/22/2024
Latest Refusal
5/22/2023
Earliest Refusal

Score Breakdown

Violation Severity
62.5×40%
Refusal Volume
25.9×30%
Recency
60.6×20%
Frequency
40.0×10%
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

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).

32803×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

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).

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

Refusal History

DateProductViolationsDivision
1/22/2024
53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
1/22/2024
53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
1/22/2024
53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
118NOT LISTED
75UNAPPROVED
Division of Northeast Imports (DNEI)
5/22/2023
66PBY99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
2280DIRSEXMPT
3280FRNMFGREG
471CSTIC LBLG
475COSMETLBLG
75UNAPPROVED
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is SHREE JAYAKALI JADIBUTI UDHYOG P's FDA import refusal history?

SHREE JAYAKALI JADIBUTI UDHYOG P (FEI: 3013360537) has 4 FDA import refusal record(s) in our database, spanning from 5/22/2023 to 1/22/2024.

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. SHREE JAYAKALI JADIBUTI UDHYOG P's FEI number is 3013360537.

What types of violations has SHREE JAYAKALI JADIBUTI UDHYOG P received?

SHREE JAYAKALI JADIBUTI UDHYOG P 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 SHREE JAYAKALI JADIBUTI UDHYOG P come from?

All FDA import refusal data for SHREE JAYAKALI JADIBUTI UDHYOG P 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.