# FDA Inspection 1199976 - REMEDI CO., LTD. - March 17, 2023

Source: https://www.keypedia.com/records/fda_inspections/remedi-co-ltd/17b832d6-f4b0-498a-8979-d404bfe2b8de
Source feed: FDA_Inspections

> FDA Inspection 1199976 for REMEDI CO., LTD. on March 17, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199976
- Company Name: REMEDI CO., LTD.
- Inspection Date: 2023-03-17
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1199976 - 2023-03-17](https://www.keypedia.com/records/fda_inspections/remedi-co-ltd/315d5789-ce77-4b1a-afe4-1da789995834)

Company: https://www.keypedia.com/companies/remedi-co-ltd/f6b03b03-7d11-40cc-a85c-17571ede76c5

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