FDA Inspection 1066596 — Ajex Meditech Ltd

Ajex Meditech Ltd — FEI 3005406104

The FDA completed an inspection of Ajex Meditech Ltd on July 12, 2018 in Suwon. 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
July 12, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Suwon (Korea (the Republic of))