FDA Inspection 1179878 — LASER LIPO LIMITED

LASER LIPO LIMITED — FEI 3010497317

The FDA completed an inspection of LASER LIPO LIMITED on Aug 18, 2022 in Edenbridge. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 18, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Edenbridge (United Kingdom)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.