Kerger & Co Bv
⚠️ Moderate Risk
FEI: 3001185380 • Schiedam, Zuid-Holland • NETHERLANDS
FEI Number
3001185380
Location
Schiedam, Zuid-Holland
Country
NETHERLANDSAddress
Fokkerstraat 515, , Schiedam, Zuid-Holland, Netherlands
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.
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 |
|---|---|---|---|
| 6/16/2022 | 95RIHMETAL HALIDE LAMP, OTHER | 47NON STD | Division of Southwest Imports (DSWI) |
| 9/23/2019 | 95RGPBLACK LIGHT, ULTRAVIOLET COMMERCIAL/CONSUMER | 476NO REGISTR | Division of Southwest Imports (DSWI) |
| 12/4/2003 | 95U28MERCURY VAPOR LAMP FOR NON-MEDICAL USE | Southwest Import District Office (SWI-DO) | |
| 12/4/2003 | 95U28MERCURY VAPOR LAMP FOR NON-MEDICAL USE | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Kerger & Co Bv's FDA import refusal history?
Kerger & Co Bv (FEI: 3001185380) has 4 FDA import refusal record(s) in our database, spanning from 12/4/2003 to 6/16/2022.
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. Kerger & Co Bv's FEI number is 3001185380.
What types of violations has Kerger & Co Bv received?
Kerger & Co Bv 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 Kerger & Co Bv come from?
All FDA import refusal data for Kerger & Co Bv 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.