FDA inspection

Catalent Anagni SRL: FDA inspection ending Jan 20, 2026

FDA inspection 1304384 · No Action Indicated (NAI) · Anagni

Key facts

Inspection ID 1304384
Firm Catalent Anagni SRL
FEI number 3002806546
Address Fontana Del Ceraso, Strada Provinciale 12 Casalina 41
City Anagni
Country Italy
Fiscal year 2026
Inspection end date Jan 20, 2026
Classification No Action Indicated (NAI)
Project area Vaccines and Allergenic Products
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
  • 10–99 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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