FDA Inspection
Defibtech, LLCDefibtech, LLC – FDA Inspection, Aug 18, 2010
Record Details
This FDA Inspection record concerns Defibtech, LLC, with an inspection on August 18, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Defibtech, LLC
- Inspection Date
- August 18, 2010
- Product Type
- Devices
View Company Profile
ID · 81857c49-3f12-445f-916c-639724f733b1
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 675878
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Defibtech, LLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 16, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 25, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 21, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 8, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Defibtech, LLC
- FDA Inspection 1024269 - 2017-08-16
- FDA Inspection 876495 - 2014-04-25
- FDA Inspection 760057 - 2011-12-21
- FDA Inspection 708589 - 2011-02-08
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.