FDA Inspection
Kub Technologies, Inc.Kub Technologies, Inc. – FDA Inspection, Feb 23, 2017
Record Details
This FDA Inspection record concerns Kub Technologies, Inc., with an inspection on February 23, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ce77b365-5406-439d-a0d1-33c8e571a9f3
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1002194
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.184Lack of or inadequate DHR procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
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Other FDA inspections of Kub Technologies, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| December 19, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 16, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 17, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 18, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kub Technologies, Inc.
- FDA Inspection 1234862 - 2024-12-19
- FDA Inspection 1097256 - 2019-07-16
- FDA Inspection 833233 - 2013-05-17
- FDA Inspection 635740 - 2009-12-18
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