FDA Inspection
Genesis Biosystems, IncFDA Inspection 1028385 - Genesis Biosystems, Inc - August 31, 2017
Record Details
This FDA Inspection record concerns Genesis Biosystems, Inc, with an inspection on August 31, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Genesis Biosystems, Inc
- Inspection Date
- August 31, 2017
- Product Type
- Devices
View Company Profile
ID · 9dab9818-70aa-4346-aaa4-1b2465373a3e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1028385
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Genesis Biosystems, Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 9, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 1, 2015 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 16, 2014 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 27, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Genesis Biosystems, Inc
- FDA Inspection 1195256 - 2023-01-09
- FDA Inspection 928343 - 2015-06-01
- FDA Inspection 908043 - 2014-12-16
- FDA Inspection 838279 - 2013-06-27
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