Panasonic Corporation
⚠️ Moderate Risk
FEI: 3007189909 • Osakaosaka • JAPAN
FEI Number
3007189909
Location
Osakaosaka
Country
JAPANAddress
2-1-61,Shiromi,Chuo-Kuobp Panasonic, , Osakaosaka, , 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
NON STD
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/6/2009 | 95RFWDVD, DVD-ROM PLAYER, LASER UTILITY/PERIPHERAL LASER PRODUCTS | 47NON STD | Florida District Office (FLA-DO) |
| 1/12/2009 | 95RFWDVD, DVD-ROM PLAYER, LASER UTILITY/PERIPHERAL LASER PRODUCTS | 47NON STD | Division of Southeast Imports (DSEI) |
| 1/12/2009 | 96RCRMICROWAVE OVEN, CONSUMER (FOOD PREP) | 47NON STD | Division of Southeast Imports (DSEI) |
| 12/4/2008 | 95RFWDVD, DVD-ROM PLAYER, LASER UTILITY/PERIPHERAL LASER PRODUCTS | 47NON STD | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Panasonic Corporation's FDA import refusal history?
Panasonic Corporation (FEI: 3007189909) has 4 FDA import refusal record(s) in our database, spanning from 12/4/2008 to 2/6/2009.
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. Panasonic Corporation's FEI number is 3007189909.
What types of violations has Panasonic Corporation received?
Panasonic Corporation 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 Panasonic Corporation come from?
All FDA import refusal data for Panasonic Corporation 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.