FDA Inspection 1135007 — Lapicor BVBA

Lapicor BVBA — FEI 1000547048

The FDA completed an inspection of Lapicor BVBA on August 14, 2020 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
August 14, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Landen (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)