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Bentley Laboratories LLC

✅ Low Risk

FEI: 2222033 • Clifton, NJ • UNITED STATES

FEI

FEI Number

2222033

📍

Location

Clifton, NJ

🇺🇸
🏢

Address

93 Entin Rd Ste 4, , Clifton, NJ, United States

Low Risk

FDA Import Risk Assessment

23.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
10/7/2013
Latest Refusal
10/7/2013
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

4712×

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.

4732×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
10/7/2013
53LC99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
473LABELING
New York District Office (NYK-DO)
10/7/2013
53LG08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
473LABELING
New York District Office (NYK-DO)

Frequently Asked Questions

What is Bentley Laboratories LLC's FDA import refusal history?

Bentley Laboratories LLC (FEI: 2222033) has 2 FDA import refusal record(s) in our database, spanning from 10/7/2013 to 10/7/2013.

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. Bentley Laboratories LLC's FEI number is 2222033.

What types of violations has Bentley Laboratories LLC received?

Bentley Laboratories LLC has been cited for 2 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 Bentley Laboratories LLC come from?

All FDA import refusal data for Bentley Laboratories LLC 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.