# FDA Inspection 776301 - Bionetek Corporation - April 10, 2012

Source: https://www.keypedia.com/records/fda_inspections/bionetek-corporation/bc735850-9ceb-41e2-9979-b14a2128ce42
Source feed: FDA_Inspections

> FDA Inspection 776301 for Bionetek Corporation on April 10, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 776301
- Company Name: Bionetek Corporation
- Inspection Date: 2012-04-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 776301 - 2012-04-10](https://www.keypedia.com/records/fda_inspections/bionetek-corporation/31fb87cb-b385-4906-8952-63d6e6263dda)
- [FDA Inspection 708055 - 2011-01-27](https://www.keypedia.com/records/fda_inspections/bionetek-corporation/aec61a02-c636-41dd-aadb-b7ad6141e446)
- [FDA Inspection 708055 - 2011-01-27](https://www.keypedia.com/records/fda_inspections/bionetek-corporation/54f35333-3a07-4c25-8701-ded712554144)

Company: https://www.keypedia.com/companies/bionetek-corporation/9cbfafde-6b92-429b-88ed-212873628310

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