FDA Inspection 854720 — Medicrea International

Medicrea International — FEI 1000432246

The FDA completed an inspection of Medicrea International on Jun 20, 2013 in Rillieux-la-pape. 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: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 20, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Rillieux-la-pape (France)

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