FDA Inspection 981516 — Herniamesh S.R.L

Herniamesh S.R.L — FEI 3005404334

The FDA completed an inspection of Herniamesh S.R.L on Jul 1, 2016 in Chivasso. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jul 1, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chivasso (Italy)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation

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