FDA Inspection
Genadyne Biotechnologies, Inc.Genadyne Biotechnologies, Inc. – FDA Inspection, Apr 27, 2016
Record Details
This FDA Inspection record concerns Genadyne Biotechnologies, Inc., with an inspection on April 27, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- April 27, 2016
- Product Type
- Devices
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ID · dfe15801-0b92-48c8-9634-e6edb3e79941
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 970698
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Complaints
- 21 CFR 820.184DHR content
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Other FDA inspections of Genadyne Biotechnologies, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| October 15, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 20, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 10, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Genadyne Biotechnologies, Inc.
- FDA Inspection 851944 - 2013-10-15
- FDA Inspection 706684 - 2011-01-20
- FDA Inspection 561876 - 2009-02-10
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