Sanmina Corporation
⚠️ Moderate Risk
FEI: 1037998 • Huntsville, AL • UNITED STATES
FEI Number
1037998
Location
Huntsville, AL
Country
UNITED STATESAddress
13000 Memorial Pkwy Sw, , Huntsville, AL, 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
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).
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/15/2016 | 75NBWSYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER | 118NOT LISTED | Detroit District Office (DET-DO) |
| 8/24/2011 | 75NBWSYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER | 16DIRECTIONS | New Orleans District Office (NOL-DO) |
| 4/26/2006 | 75JJEANALYZER, CHEMISTRY (PHOTOMETRIC, DISCRETE) FOR CLINICAL USE | 118NOT LISTED | Atlanta District Office (ATL-DO) |
Frequently Asked Questions
What is Sanmina Corporation's FDA import refusal history?
Sanmina Corporation (FEI: 1037998) has 3 FDA import refusal record(s) in our database, spanning from 4/26/2006 to 9/15/2016.
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. Sanmina Corporation's FEI number is 1037998.
What types of violations has Sanmina Corporation received?
Sanmina Corporation 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 Sanmina Corporation come from?
All FDA import refusal data for Sanmina 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.