FDA Inspection 1004993 — Haupt Pharma Latina Srl

Haupt Pharma Latina Srl — FEI 3007687501

The FDA completed an inspection of Haupt Pharma Latina Srl on Dec 16, 2016 in Latina. 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
Dec 16, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Latina (Italy)

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