CreAgri, Inc.
✅ Low Risk
FEI: 3004282947 • Newark, CA • UNITED STATES
FEI Number
3004282947
Location
Newark, CA
Country
UNITED STATESAddress
37420 Cedar Blvd Ste C, , Newark, CA, United States
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/7/2014 | 54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 473LABELING | Philadelphia District Office (PHI-DO) |
Frequently Asked Questions
What is CreAgri, Inc.'s FDA import refusal history?
CreAgri, Inc. (FEI: 3004282947) has 1 FDA import refusal record(s) in our database, spanning from 7/7/2014 to 7/7/2014.
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. CreAgri, Inc.'s FEI number is 3004282947.
What types of violations has CreAgri, Inc. received?
CreAgri, Inc. 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 CreAgri, Inc. come from?
All FDA import refusal data for CreAgri, Inc. 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.