FDA Inspection 744980 — Archimica S.p.A

Archimica S.p.A — FEI 3002874947

The FDA completed an inspection of Archimica S.p.A on September 8, 2011 in Lodi. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 8, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lodi (Italy)