# FDA Inspection 1200952 - Yoshida Denzai Kogyo Co. Ltd - March 23, 2023

Source: https://www.keypedia.com/records/fda_inspections/yoshida-denzai-kogyo-co-ltd/45801ade-08af-4f6c-b690-b770becf974c
Source feed: FDA_Inspections

> FDA Inspection 1200952 for Yoshida Denzai Kogyo Co. Ltd on March 23, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200952
- Company Name: Yoshida Denzai Kogyo Co. Ltd
- Inspection Date: 2023-03-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1200952 - 2023-03-23](https://www.keypedia.com/records/fda_inspections/yoshida-denzai-kogyo-co-ltd/62c6a4c6-b007-4d37-933c-7876de4197d6)

Company: https://www.keypedia.com/companies/yoshida-denzai-kogyo-co-ltd/966b2bd5-af15-454c-abc0-53fbd2d1961b

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