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Eli Lilly South Africa

⚠️ Moderate Risk

FEI: 3012107151 • Bryanston • SOUTH AFRICA

FEI

FEI Number

3012107151

📍

Location

Bryanston

🇿🇦
🏢

Address

35 Ballyclaire Drive, , Bryanston, , South Africa

Moderate Risk

FDA Import Risk Assessment

38.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
5/10/2017
Latest Refusal
5/10/2017
Earliest Refusal

Score Breakdown

Violation Severity
85.0×40%
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

271×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

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
5/10/2017
64RDY21SOMATROPIN (HORMONE)
27DRUG GMPS
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Eli Lilly South Africa's FDA import refusal history?

Eli Lilly South Africa (FEI: 3012107151) has 1 FDA import refusal record(s) in our database, spanning from 5/10/2017 to 5/10/2017.

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. Eli Lilly South Africa's FEI number is 3012107151.

What types of violations has Eli Lilly South Africa received?

Eli Lilly South Africa 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 Eli Lilly South Africa come from?

All FDA import refusal data for Eli Lilly South Africa 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.