FDA Inspection
Genadyne Biotechnologies, Inc.Genadyne Biotechnologies, Inc. – FDA Inspection, Feb 10, 2009
Record Details
This FDA Inspection record concerns Genadyne Biotechnologies, Inc., with an inspection on February 10, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 10, 2009
- Product Type
- Devices
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ID · d66e0e6f-1bb5-42ab-90ec-a7e4fd1e830f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 561876
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Complete files maintained
- 21 CFR 820.40(a)Document locations, Dissemination, etc.
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Other FDA inspections of Genadyne Biotechnologies, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 27, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| 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 |
Other documents for Genadyne Biotechnologies, Inc.
- FDA Inspection 970698 - 2016-04-27
- FDA Inspection 851944 - 2013-10-15
- FDA Inspection 706684 - 2011-01-20
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