Smithkline Beecham Nexico S.A. De C.V.
⚠️ Moderate Risk
FEI: 3003831271 • Mor. • MEXICO
FEI Number
3003831271
Location
Mor.
Country
MEXICOAddress
Calle 21 No. 104 Civac, , Julietec, Mor., , Mexico
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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
Frequently Asked Questions
What is Smithkline Beecham Nexico S.A. De C.V.'s FDA import refusal history?
Smithkline Beecham Nexico S.A. De C.V. (FEI: 3003831271) has 1 FDA import refusal record(s) in our database, spanning from 3/10/2003 to 3/10/2003.
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. Smithkline Beecham Nexico S.A. De C.V.'s FEI number is 3003831271.
What types of violations has Smithkline Beecham Nexico S.A. De C.V. received?
Smithkline Beecham Nexico S.A. De C.V. 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 Smithkline Beecham Nexico S.A. De C.V. come from?
All FDA import refusal data for Smithkline Beecham Nexico S.A. De C.V. 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.