NOVAPRO CO. LTD.
⚠️ Moderate Risk
FEI: 3007842555 • Zibo, Shandong • CHINA
FEI Number
3007842555
Location
Zibo, Shandong
Country
CHINAAddress
Lot 4, No. 21 Qingtian Road; Linzi, Zibo, Shandong, China
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
FALSE
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.
HOLES
The quality of the article falls below that which it purports or is represented to possess, in that the devices contain defects/holes.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/12/2018 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 223FALSE | Division of West Coast Imports (DWCI) |
| 12/12/2018 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 223FALSE | Division of West Coast Imports (DWCI) |
| 12/12/2018 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 223FALSE | Division of West Coast Imports (DWCI) |
| 4/29/2010 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 477HOLES | New York District Office (NYK-DO) |
Frequently Asked Questions
What is NOVAPRO CO. LTD.'s FDA import refusal history?
NOVAPRO CO. LTD. (FEI: 3007842555) has 4 FDA import refusal record(s) in our database, spanning from 4/29/2010 to 12/12/2018.
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. NOVAPRO CO. LTD.'s FEI number is 3007842555.
What types of violations has NOVAPRO CO. LTD. received?
NOVAPRO CO. LTD. 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 NOVAPRO CO. LTD. come from?
All FDA import refusal data for NOVAPRO CO. LTD. 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.