ACHE LABORATORIOS FARMACEUTICOSSA
⚠️ High Risk
FEI: 3015160022 • Sao Paulo • BRAZIL
FEI Number
3015160022
Location
Sao Paulo
Country
BRAZILAddress
Avenida Das Nacoes Unidas, , Sao Paulo, , Brazil
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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 ACHE LABORATORIOS FARMACEUTICOSSA's FDA import refusal history?
ACHE LABORATORIOS FARMACEUTICOSSA (FEI: 3015160022) has 3 FDA import refusal record(s) in our database, spanning from 7/31/2023 to 1/9/2026.
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. ACHE LABORATORIOS FARMACEUTICOSSA's FEI number is 3015160022.
What types of violations has ACHE LABORATORIOS FARMACEUTICOSSA received?
ACHE LABORATORIOS FARMACEUTICOSSA 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 ACHE LABORATORIOS FARMACEUTICOSSA come from?
All FDA import refusal data for ACHE LABORATORIOS FARMACEUTICOSSA 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.