FDA Inspection 844981 — LASER LIPO LIMITED

LASER LIPO LIMITED — FEI 3010497317

The FDA completed an inspection of LASER LIPO LIMITED on July 5, 2013 in Edenbridge. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 5, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Edenbridge (United Kingdom)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
1451121 CFR 812.2(b)Abbreviated requirements / non-significant risk study