FDA Inspection 1066964 — LILMO Ltd.

LILMO Ltd. — FEI 3010872792

The FDA completed an inspection of LILMO Ltd. on Sep 12, 2018 in Pamplemousses. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 12, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Pamplemousses (Mauritius)