FDA Inspection 803995 — Angiologica B.M. S.r.l.

Angiologica B.M. S.r.l. — FEI 3004874087

The FDA completed an inspection of Angiologica B.M. S.r.l. on October 25, 2012 in San Martino Siccomario. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 25, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Martino Siccomario (Italy)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
333121 CFR 820.181DMR - not or inadequately maintained
369621 CFR 820.100(b)Documentation
54621 CFR 820.75(a)Lack of or inadequate process validation