Hewlett Packard Co
⚠️ Moderate Risk
FEI: 1000221324 • Palo Alto, CA • UNITED STATES
FEI Number
1000221324
Location
Palo Alto, CA
Country
UNITED STATESAddress
3000 Hanover St, , Palo Alto, CA, United States
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.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
FAILS STD
The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
NO REGISTR
The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/19/2023 | 90JAKSYSTEM, X-RAY, TOMOGRAPHY, COMPUTED | Division of Northern Border Imports (DNBI) | |
| 10/1/2008 | 95L30LASER PRINTERS | 476NO REGISTR | Division of Southeast Imports (DSEI) |
| 9/3/2008 | 95L30LASER PRINTERS | 47NON STD | Florida District Office (FLA-DO) |
| 9/3/2008 | 95RFTLASER PRINTER, UTILITY/PERIPHERAL LASER | 47NON STD | Florida District Office (FLA-DO) |
| 9/13/2005 | 95L22LASER PRODUCT FOR NON-MEDICAL USE | 126FAILS STD | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Hewlett Packard Co's FDA import refusal history?
Hewlett Packard Co (FEI: 1000221324) has 5 FDA import refusal record(s) in our database, spanning from 9/13/2005 to 1/19/2023.
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. Hewlett Packard Co's FEI number is 1000221324.
What types of violations has Hewlett Packard Co received?
Hewlett Packard Co has been cited for 5 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 Hewlett Packard Co come from?
All FDA import refusal data for Hewlett Packard Co 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.