FDA Inspection 1113055 — Bistos Co Ltd
The FDA completed an inspection of Bistos Co Ltd on November 7, 2019 in Yongin. 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
- November 7, 2019
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Yongin (Korea (the Republic of))