FDA inspection

Catalent Pharma Solutions, LLC: FDA inspection ending Dec 17, 2025

FDA inspection 1297392 · No Action Indicated (NAI) · Philadelphia, PA

Key facts

Inspection ID 1297392
Firm Catalent Pharma Solutions, LLC
FEI number 3007617094
Address 10381 Decatur Rd
City Philadelphia
State PA
ZIP 19154
Country United States
Fiscal year 2026
Inspection end date Dec 17, 2025
Classification No Action Indicated (NAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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