FDA Inspection 748191 — Lapicor BVBA

Lapicor BVBA — FEI 1000547048

The FDA completed an inspection of Lapicor BVBA on September 15, 2011 in Landen. 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 15, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Landen (Belgium)