# FDA Inspection 893459 - Bonart Co., Ltd. - July 22, 2014

Source: https://www.keypedia.com/records/fda_inspections/bonart-co-ltd/67c09400-32c4-4a6e-858f-3650d595a012
Source feed: FDA_Inspections

> FDA Inspection 893459 for Bonart Co., Ltd. on July 22, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 893459
- Company Name: Bonart Co., Ltd.
- Inspection Date: 2014-07-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 729255 - 2011-04-21](https://www.keypedia.com/records/fda_inspections/bonart-co-ltd/33c43f69-aa74-4b19-83f0-b9de84e81706)
- [FDA Inspection 729255 - 2011-04-21](https://www.keypedia.com/records/fda_inspections/bonart-co-ltd/5fddc0bd-d697-4dc6-848c-3ede059576a3)

Company: https://www.keypedia.com/companies/bonart-co-ltd/e7bf60ff-b5b3-4cda-a3cf-00119fcd5d8e

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