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Chordia R

⚠️ Moderate Risk

FEI: 3004431260 • Pune • INDIA

FEI

FEI Number

3004431260

📍

Location

Pune

🇮🇳

Country

INDIA
🏢

Address

389 Pioneer Medicals, , Pune, , India

Moderate Risk

FDA Import Risk Assessment

33.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
3/14/2005
Latest Refusal
3/14/2005
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

1793×

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
3/14/2005
61PCA09GLIPIZIDE (ANTI-DIABETIC)
179AGR RX
New Orleans District Office (NOL-DO)
3/14/2005
61PCN17INSULIN (INJ) (ANTI-DIABETIC)
179AGR RX
New Orleans District Office (NOL-DO)
3/14/2005
62OCA14AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II)
179AGR RX
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Chordia R's FDA import refusal history?

Chordia R (FEI: 3004431260) has 3 FDA import refusal record(s) in our database, spanning from 3/14/2005 to 3/14/2005.

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. Chordia R's FEI number is 3004431260.

What types of violations has Chordia R received?

Chordia R 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 Chordia R come from?

All FDA import refusal data for Chordia R 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.