FDA Inspection 841020 — Serf

Serf — FEI 3008668801

The FDA completed an inspection of Serf on June 20, 2013 in Decines-Charpieu. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 20, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Decines-Charpieu (France)

Citations

IDCFRDescription
255721 CFR 820.30(c)Design input - documentation
313021 CFR 820.100(a)Lack of or inadequate procedures