FDA Inspection 1125050 — Hikma Farmaceutica, (Portugal) S.A.

Hikma Farmaceutica, (Portugal) S.A. — FEI 3002807173

The FDA completed an inspection of Hikma Farmaceutica, (Portugal) S.A. on March 6, 2020 in Terrugem Snt. 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
March 6, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Terrugem Snt (Portugal)

Additional Details

Mutual Recognition Agreement (MRA)