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Albert David Ltd.

⚠️ Moderate Risk

FEI: 1000175804 • Kolkata, West Bengal • INDIA

FEI

FEI Number

1000175804

📍

Location

Kolkata, West Bengal

🇮🇳

Country

INDIA
🏢

Address

15 Chittaranjan Avenue, , Kolkata, West Bengal, India

Moderate Risk

FDA Import Risk Assessment

37.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
3/8/2005
Latest Refusal
3/8/2005
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

1153×

DR QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to be represented as a drug the name of which is recognized in an official compendium and its strength appears to differ from or its quality or purity appear to fall below the standards set forth in such compendium.

Refusal History

DateProductViolationsDivision
3/8/2005
61PAY04CHLORPROPAMIDE (ANTI-DIABETIC)
115DR QUALITY
New York District Office (NYK-DO)
3/8/2005
61PAY04CHLORPROPAMIDE (ANTI-DIABETIC)
115DR QUALITY
New York District Office (NYK-DO)
3/8/2005
61PAY04CHLORPROPAMIDE (ANTI-DIABETIC)
115DR QUALITY
New York District Office (NYK-DO)

Frequently Asked Questions

What is Albert David Ltd.'s FDA import refusal history?

Albert David Ltd. (FEI: 1000175804) has 3 FDA import refusal record(s) in our database, spanning from 3/8/2005 to 3/8/2005.

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. Albert David Ltd.'s FEI number is 1000175804.

What types of violations has Albert David Ltd. received?

Albert David Ltd. 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 Albert David Ltd. come from?

All FDA import refusal data for Albert David 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.