FDA Inspection 1026454 — InBody Co., Ltd.
The FDA completed an inspection of InBody Co., Ltd. on August 10, 2017 in Cheonan. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- August 10, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Cheonan (Korea (the Republic of))