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Hpl

⚠️ Moderate Risk

FEI: 3007730718 • Kolkata, West Bengal • INDIA

FEI

FEI Number

3007730718

📍

Location

Kolkata, West Bengal

🇮🇳

Country

INDIA
🏢

Address

1 Auckland Place, , Kolkata, West Bengal, India

Moderate Risk

FDA Import Risk Assessment

47.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
9/8/2009
Latest Refusal
9/8/2009
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

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).

Refusal History

DateProductViolationsDivision
9/8/2009
60XCA17ATENOLOL (ANTI-ADRENERGIC)
75UNAPPROVED
Cincinnati District Office (CIN-DO)
9/8/2009
63ACA07RISEDRONATE SODIUM (BONE CALCIUM REGULATOR)
75UNAPPROVED
Cincinnati District Office (CIN-DO)
9/8/2009
62OCA14AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II)
75UNAPPROVED
Cincinnati District Office (CIN-DO)
9/8/2009
54BBE01CALCIUM (MINERAL)
75UNAPPROVED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Hpl's FDA import refusal history?

Hpl (FEI: 3007730718) has 4 FDA import refusal record(s) in our database, spanning from 9/8/2009 to 9/8/2009.

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. Hpl's FEI number is 3007730718.

What types of violations has Hpl received?

Hpl 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 Hpl come from?

All FDA import refusal data for Hpl 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.