FDA Inspection 1028720 — Alban Muller International

Alban Muller International — FEI 3002656672

The FDA completed an inspection of Alban Muller International on September 22, 2017 in Fontenay-Sur-Eure. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 22, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fontenay-Sur-Eure (France)