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Teva Branded Pharmaceutical Products R&D, Inc.

⚠️ Moderate Risk

FEI: 1000307054 • Malvern, PA • UNITED STATES

FEI

FEI Number

1000307054

📍

Location

Malvern, PA

🇺🇸
🏢

Address

2 W Liberty Blvd Ste 300, , Malvern, PA, United States

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
8/31/2004
Latest Refusal
8/31/2004
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

1791×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

Refusal History

DateProductViolationsDivision
8/31/2004
66BIY26NIKETHAMIDE (STIMULANT)
179AGR RX
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Teva Branded Pharmaceutical Products R&D, Inc.'s FDA import refusal history?

Teva Branded Pharmaceutical Products R&D, Inc. (FEI: 1000307054) has 1 FDA import refusal record(s) in our database, spanning from 8/31/2004 to 8/31/2004.

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. Teva Branded Pharmaceutical Products R&D, Inc.'s FEI number is 1000307054.

What types of violations has Teva Branded Pharmaceutical Products R&D, Inc. received?

Teva Branded Pharmaceutical Products R&D, Inc. 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 Teva Branded Pharmaceutical Products R&D, Inc. come from?

All FDA import refusal data for Teva Branded Pharmaceutical Products R&D, Inc. 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.