FDA inspection

Catalent Indiana, LLC: FDA inspection ending Aug 3, 2018

FDA inspection 1063669 · No Action Indicated (NAI) · Bloomington, IN

Key facts

Inspection ID 1063669
Firm Catalent Indiana, LLC
FEI number 3005949964
Address 1300 S Patterson Dr
City Bloomington
State IN
ZIP 47403
Country United States
Fiscal year 2018
Inspection end date Aug 3, 2018
Classification No Action Indicated (NAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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