FDA Inspection 990212 — Guerbet Ireland Unlimited Company

Guerbet Ireland Unlimited Company — FEI 1000588788

The FDA completed an inspection of Guerbet Ireland Unlimited Company on June 3, 2016 in Dublin 15. 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
June 3, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dublin 15 (Ireland)