FDA Inspection 1207926 — Lorem Cytori USA

Lorem Cytori USA — FEI 3016774639

The FDA completed an inspection of Lorem Cytori USA on May 19, 2023 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 19, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)