# REMEDI CO., LTD. – FDA Inspection, Mar 17, 2023

Source: https://www.keypedia.com/records/fda_inspections/remedi-co-ltd/315d5789-ce77-4b1a-afe4-1da789995834
Source feed: FDA_Inspections

> FDA inspection 1199976 of REMEDI CO., LTD., March 17, 2023. Classification: No Action Indicated (NAI). Form 483 issued.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Investigator](https://www.keypedia.com/people/preston-m-lee/e44adac3-a915-4bfb-8b06-a41ea5803358)

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