FDA Inspection 1050432 — Multimedical S.R.L.

Multimedical S.R.L. — FEI 3005622231

The FDA completed an inspection of Multimedical S.R.L. on Apr 19, 2018 in Viadana. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 19, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Viadana (Italy)

Citations

IDCFRDescription
311921 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
313021 CFR 820.100(a)Lack of or inadequate procedures

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