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SANOFI-SYNTHELABO INC

✅ Low Risk

FEI: 3016756300 • Panama City • PANAMA

FEI

FEI Number

3016756300

📍

Location

Panama City

🇵🇦

Country

PANAMA
🏢

Address

Piso 32, Torre Evolution, Panama City, , Panama

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
1
Unique Violations
5/15/2020
Latest Refusal
5/15/2020
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
5/15/2020
62LDY29HYDROXYCHLOROQUINE SULFATE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SANOFI-SYNTHELABO INC's FDA import refusal history?

SANOFI-SYNTHELABO INC (FEI: 3016756300) has 1 FDA import refusal record(s) in our database, spanning from 5/15/2020 to 5/15/2020.

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. SANOFI-SYNTHELABO INC's FEI number is 3016756300.

What types of violations has SANOFI-SYNTHELABO INC received?

SANOFI-SYNTHELABO 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 SANOFI-SYNTHELABO INC come from?

All FDA import refusal data for SANOFI-SYNTHELABO 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.