FDA Inspection 1061068 — Catalent Belgium SA
The FDA completed an inspection of Catalent Belgium SA on July 31, 2018 in Brussels. 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
- July 31, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Brussels (Belgium)