FDA Inspection 958331 — Handicare Usa Inc

Handicare Usa Inc — FEI 3007802293

The FDA completed an inspection of Handicare Usa Inc on Jan 27, 2016 in Maryland Heights, MO. 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
Jan 27, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Maryland Heights, MO (United States)