# FDA Inspection 1026456 - Inbody Co Ltd - August 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/inbody-co-ltd/5cf19c94-2265-4bef-9e7f-45acad28e783
Source feed: FDA_Inspections

> FDA Inspection 1026456 for Inbody Co Ltd on August 10, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026456
- Company Name: Inbody Co Ltd
- Inspection Date: 2017-08-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/inbody-co-ltd/0af8acb8-5aaa-455b-9d24-eba09d96951e

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