Fresh Air Inc.
⚠️ Moderate Risk
FEI: 3003333003 • Fukuoka, Fukuoka • JAPAN
FEI Number
3003333003
Location
Fukuoka, Fukuoka
Country
JAPANAddress
Enokida Hakata, 2chome-8-35; Enokida; Hakata, Fukuoka, Fukuoka, Japan
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.
Refusal History
Frequently Asked Questions
What is Fresh Air Inc.'s FDA import refusal history?
Fresh Air Inc. (FEI: 3003333003) has 2 FDA import refusal record(s) in our database, spanning from 8/26/2004 to 8/26/2004.
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. Fresh Air Inc.'s FEI number is 3003333003.
What types of violations has Fresh Air Inc. received?
Fresh Air 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 Fresh Air Inc. come from?
All FDA import refusal data for Fresh Air 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.