FDA inspection

Mylan Teoranta: FDA inspection ending Jun 15, 2016

FDA inspection 978312 · No Action Indicated (NAI) · Inverin

Key facts

Inspection ID 978312
Firm Mylan Teoranta
FEI number 3002806521
Address Kilroe East
City Inverin
Country Ireland
Fiscal year 2016
Inspection end date Jun 15, 2016
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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