# BONART CO. LTD. – FDA Inspection, Apr 21, 2011

Source: https://www.keypedia.com/records/fda_inspections/bonart-co-ltd/fa3820b4-62b1-402c-9497-7708c04c0a3a
Source feed: FDA_Inspections

> FDA inspection 734366 of BONART CO. LTD., April 21, 2011. Classification: Official Action Indicated (OAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 734366
- Company Name: BONART CO. LTD.
- Inspection Date: 2011-04-21
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- 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 891962 - 2014-07-17](https://www.keypedia.com/records/fda_inspections/bonart-co-ltd/61c5f94c-0a8e-44e2-80fa-0f0293f48854)

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

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