FDA Inspection 1008927 — Laboratorios Zepol S.A.

Laboratorios Zepol S.A. — FEI 3004637474

The FDA completed an inspection of Laboratorios Zepol S.A. on March 29, 2017 in Curridabat. 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 29, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Curridabat (Costa Rica)