FDA Inspection 1094988 — Archimica S.P.A

Archimica S.P.A — FEI 3002874947

The FDA completed an inspection of Archimica S.P.A on Jul 21, 2017 in Lodi. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.