FDA inspection

Janssen Cilag Manufacturing LLC: FDA inspection ending Feb 18, 2011

FDA inspection 714921 · No Action Indicated (NAI) · Gurabo, PR

Key facts

Inspection ID 714921
Firm Janssen Cilag Manufacturing LLC
FEI number 3006244497
Address State Road 933 Km. 0.1, Mamey Ward
City Gurabo
State PR
ZIP 00778
Country United States
Fiscal year 2011
Inspection end date Feb 18, 2011
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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