# FDA Inspection 708055 - Bionetek Corporation - January 27, 2011

Source: https://www.keypedia.com/records/fda_inspections/bionetek-corporation/54f35333-3a07-4c25-8701-ded712554144
Source feed: FDA_Inspections

> FDA Inspection 708055 for Bionetek Corporation on January 27, 2011. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 708055
- Company Name: Bionetek Corporation
- Inspection Date: 2011-01-27
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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