FDA Inspection 1252977 — Catalent Maryland Inc

Catalent Maryland Inc — FEI 3015434301

The FDA completed an inspection of Catalent Maryland Inc on November 15, 2024 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
November 15, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Harmans, MD (United States)