FDA Inspection 1063847 — Mattioli Engineering Italia SpA

Mattioli Engineering Italia SpA — FEI 1000390170

The FDA completed an inspection of Mattioli Engineering Italia SpA on Aug 30, 2018 in Calenzano. 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
Aug 30, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Calenzano (Italy)

Citations

IDCFRDescription
320721 CFR 820.50(b)Supplier notification of changes
407021 CFR 820.30(g)Design validation - documentation