FDA Inspection 1056604 — Alfasigma S.P.A.

Alfasigma S.P.A. — FEI 3002808171

The FDA completed an inspection of Alfasigma S.P.A. on Jun 21, 2018 in Pomezia. 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.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 21, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pomezia (Italy)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.