Labor Diagnostika Nord Gmbh & Co. KG
⚠️ Moderate Risk
FEI: 3003659983 • Nordhorn, Lower Saxony • GERMANY
FEI Number
3003659983
Location
Nordhorn, Lower Saxony
Country
GERMANYAddress
Am Eichenhain 1, , Nordhorn, Lower Saxony, Germany
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).
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/3/2025 | 75CHQCHROMATOGRAPHIC/FLUOROMETRIC METHOD, CATECHOLAMINES | 508NO 510(K) | Division of Northeast Imports (DNEI) |
| 9/16/2011 | 88NJTIMMUNOHISTOCHEMISTRY REAGENTS AND KITS | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 9/16/2011 | 88NJTIMMUNOHISTOCHEMISTRY REAGENTS AND KITS | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 9/16/2011 | 88NJTIMMUNOHISTOCHEMISTRY REAGENTS AND KITS | 118NOT LISTED | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Labor Diagnostika Nord Gmbh & Co. KG's FDA import refusal history?
Labor Diagnostika Nord Gmbh & Co. KG (FEI: 3003659983) has 4 FDA import refusal record(s) in our database, spanning from 9/16/2011 to 7/3/2025.
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. Labor Diagnostika Nord Gmbh & Co. KG's FEI number is 3003659983.
What types of violations has Labor Diagnostika Nord Gmbh & Co. KG received?
Labor Diagnostika Nord Gmbh & Co. KG 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 Labor Diagnostika Nord Gmbh & Co. KG come from?
All FDA import refusal data for Labor Diagnostika Nord Gmbh & Co. KG 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.