FDA Inspection
Med-Logics, Inc.Med-Logics, Inc. – FDA Inspection, Jan 12, 2009
Record Details
This FDA Inspection record concerns Med-Logics, Inc., with an inspection on January 12, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Med-Logics, Inc.
- Inspection Date
- January 12, 2009
- Product Type
- Devices
View Company Profile
ID · 8381bfce-1dfd-4cde-956c-4d2986af0d86
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 561301
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.181(a)DMR device specifications
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Med-Logics, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 18, 2024 | Not classified | Dallas District Office | |
| May 24, 2016 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 18, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Med-Logics, Inc.
- FDA Inspection 1237993 - 2024-04-18
- FDA Inspection 973096 - 2016-05-24
- FDA Inspection 786425 - 2012-05-18
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.