# Bionet Co., Ltd. – FDA Inspection, Feb 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/bionet-co-ltd/fe666d17-7320-4bde-88a0-31d947b38ec7
Source feed: FDA_Inspections

> FDA inspection 1082597 of Bionet Co., Ltd., February 21, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1082597
- Company Name: Bionet Co., Ltd.
- Inspection Date: 2019-02-21
- 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: 0

## Related Documents

- FDA Inspection 816934 - 2013-01-17
- [FDA Inspection 727569 - 2011-04-21](https://www.keypedia.com/records/fda_inspections/bionet-co-ltd/961e7115-d6ca-4e73-8358-16647655c8a1)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/christina-l-bigham/f3da8e26-4a8c-43a8-8070-349fe4500289)

Company: https://www.keypedia.com/companies/bionet-co-ltd/cc3fa3ab-ef3f-470c-9265-6522e8aefaee

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