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Johnson & Johnson

⚠️ Moderate Risk

FEI: 3006178968 • Jakarta Selatan, Dki Jakarta • INDONESIA

FEI

FEI Number

3006178968

📍

Location

Jakarta Selatan, Dki Jakarta

🇮🇩

Country

INDONESIA
🏢

Address

Jln. Mampang Raya 1, , Jakarta Selatan, Dki Jakarta, Indonesia

Moderate Risk

FDA Import Risk Assessment

27.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
11/23/2011
Latest Refusal
11/23/2011
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
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

4754×

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
11/23/2011
53AD01BABY SHAMPOO (BABY PRODUCTS)
475COSMETLBLG
New York District Office (NYK-DO)
11/23/2011
53AD02LOTIONS, OILS, POWDERS AND CREAMS (BABY PRODUCTS)
475COSMETLBLG
New York District Office (NYK-DO)
11/23/2011
53AY99OTHER BABY PRODUCTS, N.E.C.
475COSMETLBLG
New York District Office (NYK-DO)
11/23/2011
53AH02LOTIONS, OILS, POWDERS AND CREAMS (BABY PRODUCTS)
475COSMETLBLG
New York District Office (NYK-DO)

Frequently Asked Questions

What is Johnson & Johnson's FDA import refusal history?

Johnson & Johnson (FEI: 3006178968) has 4 FDA import refusal record(s) in our database, spanning from 11/23/2011 to 11/23/2011.

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. Johnson & Johnson's FEI number is 3006178968.

What types of violations has Johnson & Johnson received?

Johnson & Johnson has been cited for 1 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 Johnson & Johnson come from?

All FDA import refusal data for Johnson & Johnson 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.