Siemens Healthcare Diagnostics Manufacturing Ltd.
⚠️ Moderate Risk
FEI: 3002806693 • Sudbury, Suffolk • UNITED KINGDOM
FEI Number
3002806693
Location
Sudbury, Suffolk
Country
UNITED KINGDOMAddress
Northern Road, Chilton Industrial Estate, Sudbury, Suffolk, United Kingdom
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).
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
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.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
Frequently Asked Questions
What is Siemens Healthcare Diagnostics Manufacturing Ltd.'s FDA import refusal history?
Siemens Healthcare Diagnostics Manufacturing Ltd. (FEI: 3002806693) has 2 FDA import refusal record(s) in our database, spanning from 8/17/2004 to 10/18/2011.
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. Siemens Healthcare Diagnostics Manufacturing Ltd.'s FEI number is 3002806693.
What types of violations has Siemens Healthcare Diagnostics Manufacturing Ltd. received?
Siemens Healthcare Diagnostics Manufacturing Ltd. has been cited for 4 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 Siemens Healthcare Diagnostics Manufacturing Ltd. come from?
All FDA import refusal data for Siemens Healthcare Diagnostics Manufacturing 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.