FDA Inspection 1207147 — Catalent Maryland Inc

Catalent Maryland Inc — FEI 3015434301

The FDA completed an inspection of Catalent Maryland Inc on March 10, 2023 in Harmans, MD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 10, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Harmans, MD (United States)