FDA Inspection 1197573 — Catalent Maryland Inc

Catalent Maryland Inc — FEI 3015434301

The FDA completed an inspection of Catalent Maryland Inc on January 24, 2023 in Harmans, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 24, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Harmans, MD (United States)