FDA Inspection 1058607 — Microtek Medical Malta Limited

Microtek Medical Malta Limited — FEI 3006581049

The FDA completed an inspection of Microtek Medical Malta Limited on May 31, 2018 in Il-Mosta. 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
May 31, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Il-Mosta (Malta)