Oglesby & Butler
⚠️ Moderate Risk
FEI: 3000213454 • Carlow • IRELAND
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
NO PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/29/2010 | 80MSNCIGARETTES (CONTAINING TOBACCO) | New York District Office (NYK-DO) | |
| 11/16/2010 | 73BZEHEATER, BREATHING SYSTEM W/WO CONTROLLER (NOT HUMIDIFIER OR NEBULIZER | Philadelphia District Office (PHI-DO) | |
| 11/3/2010 | 73CADVAPORIZER, ANESTHESIA, NON-HEATED | Philadelphia District Office (PHI-DO) | |
| 10/28/2010 | 73CADVAPORIZER, ANESTHESIA, NON-HEATED | Philadelphia District Office (PHI-DO) |
Frequently Asked Questions
What is Oglesby & Butler's FDA import refusal history?
Oglesby & Butler (FEI: 3000213454) has 4 FDA import refusal record(s) in our database, spanning from 10/28/2010 to 11/29/2010.
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. Oglesby & Butler's FEI number is 3000213454.
What types of violations has Oglesby & Butler received?
Oglesby & Butler 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 Oglesby & Butler come from?
All FDA import refusal data for Oglesby & Butler 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.