FDA Inspection 628714 — Mylan Teoranta

Mylan Teoranta — FEI 3002806521

The FDA completed an inspection of Mylan Teoranta on Oct 15, 2009 in Inverin. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 15, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Inverin (Ireland)