FDA Inspection 782346 — Mylan Teoranta

Mylan Teoranta — FEI 3002806521

The FDA completed an inspection of Mylan Teoranta on Mar 30, 2012 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
Mar 30, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Inverin (Ireland)