FDA Inspection
KBD, Inc.KBD, Inc. – FDA Inspection, Jul 25, 2011
Record Details
This FDA Inspection record concerns KBD, Inc., with an inspection on July 25, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- KBD, Inc.
- Inspection Date
- July 25, 2011
- Product Type
- Devices
View Company Profile
ID · 70098056-7e41-4d5f-9cd1-39a1ade27b22
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 737794
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of KBD, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 8, 2019 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| December 23, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 22, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for KBD, Inc.
- FDA Inspection 1109206 - 2019-11-08
- FDA Inspection 998372 - 2016-12-23
- FDA Inspection 797566 - 2012-08-22
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.