FDA Inspection 981516 — Herniamesh S.r.l

Herniamesh S.r.l — FEI 3005404334

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

Inspection Details

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

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation