# FDA Inspection 1207456 - P.T. Sankei Medical Industries - May 11, 2023

Source: https://www.keypedia.com/records/fda_inspections/pt-sankei-medical-industries/6154199d-4c4d-479f-b718-b63d9cf40f00
Source feed: FDA_Inspections

> FDA Inspection 1207456 for P.T. Sankei Medical Industries on May 11, 2023. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1207456
- Company Name: P.T. Sankei Medical Industries
- Inspection Date: 2023-05-11
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1207456 - 2023-05-11](https://www.keypedia.com/records/fda_inspections/pt-sankei-medical-industries/a71bf542-7bb4-4dfc-b3e9-fd40b137bf76)
- [FDA Inspection 969061 - 2016-04-14](https://www.keypedia.com/records/fda_inspections/pt-sankei-medical-industries/779438dc-275d-4c31-af5d-d346798b04e5)

Company: https://www.keypedia.com/companies/pt-sankei-medical-industries/dc3fa15f-5914-4765-82ca-1c46477bcf51

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