FDA Inspection
KBD, Inc.KBD, Inc. – FDA Inspection, Dec 23, 2016
Record Details
This FDA Inspection record concerns KBD, Inc., with an inspection on December 23, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · bafdebed-303d-4768-8575-f492c27f6da6
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 998372
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
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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 |
| August 22, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 25, 2011 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for KBD, Inc.
- FDA Inspection 1109206 - 2019-11-08
- FDA Inspection 797566 - 2012-08-22
- FDA Inspection 737794 - 2011-07-25
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