# FDA Inspection 1113055 - Bistos Co Ltd - November 07, 2019

Source: https://www.keypedia.com/records/fda_inspections/bistos-co-ltd/3ca4749b-f13d-40f5-ba75-182fe0fcd2cb
Source feed: FDA_Inspections

> FDA Inspection 1113055 for Bistos Co Ltd on November 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1113055
- Company Name: Bistos Co Ltd
- Inspection Date: 2019-11-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1113055 - 2019-11-07](https://www.keypedia.com/records/fda_inspections/bistos-co-ltd/ba78b735-9683-496b-9a20-c9c7a84f3a7f)
- [FDA Inspection 804127 - 2012-09-27](https://www.keypedia.com/records/fda_inspections/bistos-co-ltd/0867feb3-4122-42e2-b82a-4770e4c72480)

Company: https://www.keypedia.com/companies/bistos-co-ltd/9f1d8538-bcae-4345-83aa-1e816266645c

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