FDA Inspection 751931 — Mattioli Engineering Italia SpA

Mattioli Engineering Italia SpA — FEI 1000390170

The FDA completed an inspection of Mattioli Engineering Italia SpA on Sep 29, 2011 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 29, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Calenzano (Italy)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
326321 CFR 820.250(b)Sampling plans
407021 CFR 820.30(g)Design validation - documentation