FDA Inspection 1280952 — CTL BIOTEC
The FDA completed an inspection of CTL BIOTEC on June 19, 2025 in Daegu. 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
- June 19, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Daegu (Korea (the Republic of))