# FDA Inspection 891962 - BONART CO. LTD. - July 17, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/bonart-co-ltd/61c5f94c-0a8e-44e2-80fa-0f0293f48854
Source feed: FDA_Inspections

> FDA Inspection 891962 for BONART CO. LTD. on July 17, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 891962
- Company Name: BONART CO. LTD.
- Inspection Date: 2014-07-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 734366 - 2011-04-21](https://www.globalkeysolutions.net/records/fda_inspections/bonart-co-ltd/fa3820b4-62b1-402c-9497-7708c04c0a3a)

Company: https://www.globalkeysolutions.net/companies/bonart-co-ltd/c7a0e9c8-9a7e-4eb3-8c7e-8349119a0971

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