FDA Inspection 726551 — AlbyPharma

AlbyPharma — FEI 3002806637

The FDA completed an inspection of AlbyPharma on May 18, 2010 in Clonmel. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 18, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Clonmel (Ireland)