SYMBIO-LAB SP.Z.O.O.
✅ Low Risk
FEI: 3013187448 • Krosno, Podkarpackie • POLAND
FEI Number
3013187448
Location
Krosno, Podkarpackie
Country
POLANDAddress
Ul. Joachima Lelewela 12/29, , Krosno, Podkarpackie, Poland
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
LACKS FIRM
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/8/2017 | 54ACA90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | Division of Northeast Imports (DNEI) | |
| 9/8/2017 | 54ACA99VITAMIN, N.E.C. | Division of Northeast Imports (DNEI) | |
| 9/8/2017 | 54ACA90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is SYMBIO-LAB SP.Z.O.O.'s FDA import refusal history?
SYMBIO-LAB SP.Z.O.O. (FEI: 3013187448) has 3 FDA import refusal record(s) in our database, spanning from 9/8/2017 to 9/8/2017.
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. SYMBIO-LAB SP.Z.O.O.'s FEI number is 3013187448.
What types of violations has SYMBIO-LAB SP.Z.O.O. received?
SYMBIO-LAB SP.Z.O.O. 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 SYMBIO-LAB SP.Z.O.O. come from?
All FDA import refusal data for SYMBIO-LAB SP.Z.O.O. 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.