FDA Inspection 1159849 — Astoriom Ireland Limited

Astoriom Ireland Limited — FEI 3013683912

The FDA completed an inspection of Astoriom Ireland Limited on August 7, 2019 in Tramore. 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
August 7, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tramore (Ireland)

Additional Details

Mutual Recognition Agreement (MRA)