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Synthesis

⚠️ Moderate Risk

FEI: 3005049822 • Santaf De Bogo • COLOMBIA

FEI

FEI Number

3005049822

📍

Location

Santaf De Bogo

🇨🇴

Country

COLOMBIA
🏢

Address

Carretera 44 N-M 20-73, , Santaf De Bogo, , Colombia

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
6/11/2018
Latest Refusal
6/11/2018
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

751×

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
6/11/2018
65JCB39DROSPIRENONE
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Synthesis's FDA import refusal history?

Synthesis (FEI: 3005049822) has 1 FDA import refusal record(s) in our database, spanning from 6/11/2018 to 6/11/2018.

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. Synthesis's FEI number is 3005049822.

What types of violations has Synthesis received?

Synthesis 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 Synthesis come from?

All FDA import refusal data for Synthesis 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.