FDA Inspection 1063669 — Catalent Indiana, LLC
The FDA completed an inspection of Catalent Indiana, LLC on Aug 3, 2018 in Bloomington, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 3, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Bloomington, IN (United States)