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Daiichi Sankyo, Inc.

⚠️ Moderate Risk

FEI: 3003089536 • Basking Ridge, NJ • UNITED STATES

FEI

FEI Number

3003089536

📍

Location

Basking Ridge, NJ

🇺🇸
🏢

Address

211 Mount Airy Rd, , Basking Ridge, NJ, United States

Moderate Risk

FDA Import Risk Assessment

29.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
6/7/2016
Latest Refusal
8/21/2009
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
2.9×10%
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

1792×

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
6/7/2016
62OBC14AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II)
179AGR RX
Division of Southeast Imports (DSEI)
8/21/2009
62CDA68OLMESARTAN MEDOXOMIL
179AGR RX
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Daiichi Sankyo, Inc.'s FDA import refusal history?

Daiichi Sankyo, Inc. (FEI: 3003089536) has 2 FDA import refusal record(s) in our database, spanning from 8/21/2009 to 6/7/2016.

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. Daiichi Sankyo, Inc.'s FEI number is 3003089536.

What types of violations has Daiichi Sankyo, Inc. received?

Daiichi Sankyo, 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 Daiichi Sankyo, Inc. come from?

All FDA import refusal data for Daiichi Sankyo, 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.