FDA Inspection 1015890 — Invacare Corporation

Invacare Corporation — FEI 1000220413

The FDA completed an inspection of Invacare Corporation on June 7, 2017 in North Ridgeville, OH. 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
June 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
North Ridgeville, OH (United States)