FDA inspection

Janssen - Cilag Spa.: FDA inspection ending Apr 21, 2006

FDA inspection 424666 · No Action Indicated (NAI) · Latina

Key facts

Inspection ID 424666
Firm Janssen - Cilag Spa.
FEI number 3003164454
Address Via Carlo Janssen S N
City Latina
Fiscal year 2006
Inspection end date Apr 21, 2006
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes 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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