NALPIHERBS SAS
⚠️ Moderate Risk
FEI: 3015170974 • Bogota • COLOMBIA
FEI Number
3015170974
Location
Bogota
Country
COLOMBIAAddress
Cl 23 66 46 Cs 1206, , Bogota, , Colombia
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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
MFR INJ
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (the Act) in that such article appears to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/12/2021 | 28AGC04BASIL (SWEET BASIL), WHOLE (SPICE) | Division of Northeast Imports (DNEI) | |
| 6/21/2021 | 28AGC04BASIL (SWEET BASIL), WHOLE (SPICE) | Division of Northeast Imports (DNEI) | |
| 6/2/2021 | 28AGC04BASIL (SWEET BASIL), WHOLE (SPICE) | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is NALPIHERBS SAS's FDA import refusal history?
NALPIHERBS SAS (FEI: 3015170974) has 3 FDA import refusal record(s) in our database, spanning from 6/2/2021 to 7/12/2021.
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. NALPIHERBS SAS's FEI number is 3015170974.
What types of violations has NALPIHERBS SAS received?
NALPIHERBS SAS 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 NALPIHERBS SAS come from?
All FDA import refusal data for NALPIHERBS SAS 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.