FDA Inspection 864288 — IBSA Farmaceutici Italia Srl

IBSA Farmaceutici Italia Srl — FEI 3008280916

The FDA completed an inspection of IBSA Farmaceutici Italia Srl on January 30, 2014 in Lodi. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 30, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Lodi (Italy)