Pamalat Brasil Sa Industria Alimentos
⚠️ Moderate Risk
FEI: 3003722990 • Sao Paulo, SP • BRAZIL
FEI Number
3003722990
Location
Sao Paulo, SP
Country
BRAZILAddress
Rua Tenerife 31, , Sao Paulo, SP, Brazil
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
NO PERMIT
The article of milk or cream is not accompanied by a valid import milk permit, as required by the Federal Import Milk Act (21 U.S.C. 141-149).
Refusal History
Frequently Asked Questions
What is Pamalat Brasil Sa Industria Alimentos's FDA import refusal history?
Pamalat Brasil Sa Industria Alimentos (FEI: 3003722990) has 2 FDA import refusal record(s) in our database, spanning from 9/30/2002 to 1/26/2004.
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. Pamalat Brasil Sa Industria Alimentos's FEI number is 3003722990.
What types of violations has Pamalat Brasil Sa Industria Alimentos received?
Pamalat Brasil Sa Industria Alimentos 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 Pamalat Brasil Sa Industria Alimentos come from?
All FDA import refusal data for Pamalat Brasil Sa Industria Alimentos 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.