# Genadyne Biotechnologies, Inc. – FDA Inspection, Apr 27, 2016

Source: https://www.keypedia.com/records/fda_inspections/genadyne-biotechnologies-inc/dfe15801-0b92-48c8-9634-e6edb3e79941
Source feed: FDA_Inspections

> FDA inspection 970698 of Genadyne Biotechnologies, Inc., April 27, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 970698
- Company Name: Genadyne Biotechnologies, Inc.
- Inspection Date: 2016-04-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 851944 - 2013-10-15
- FDA Inspection 706684 - 2011-01-20
- [FDA Inspection 561876 - 2009-02-10](https://www.keypedia.com/records/fda_inspections/genadyne-biotechnologies-inc/d66e0e6f-1bb5-42ab-90ec-a7e4fd1e830f)

Company: https://www.keypedia.com/companies/genadyne-biotechnologies-inc/7681abac-e709-4004-8e47-ae461777a217

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7