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Aventis Pharma SA

⚠️ Moderate Risk

FEI: 3003641053 • Unknown • GUATEMALA

FEI

FEI Number

3003641053

📍

Location

Unknown

🇬🇹

Country

GUATEMALA
🏢

Address

Unknown, , Unknown, , Guatemala

Moderate Risk

FDA Import Risk Assessment

41.6
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
4/26/2007
Latest Refusal
11/19/2003
Earliest Refusal

Score Breakdown

Violation Severity
85.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
8.7×10%
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

753×

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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

Refusal History

DateProductViolationsDivision
4/26/2007
60LAA21DIPYRONE (ANALGESIC)
75UNAPPROVED
Cincinnati District Office (CIN-DO)
4/16/2007
60LBA05ASPIRIN (ANALGESIC)
16DIRECTIONS
75UNAPPROVED
Southwest Import District Office (SWI-DO)
11/19/2003
60RIY99ANOREXIC, N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Aventis Pharma SA's FDA import refusal history?

Aventis Pharma SA (FEI: 3003641053) has 3 FDA import refusal record(s) in our database, spanning from 11/19/2003 to 4/26/2007.

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. Aventis Pharma SA's FEI number is 3003641053.

What types of violations has Aventis Pharma SA received?

Aventis Pharma SA has been cited for 2 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 Aventis Pharma SA come from?

All FDA import refusal data for Aventis Pharma SA 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.