FDA Inspection 1020854 — Storz Medical America Inc

Storz Medical America Inc — FEI 1000511585

The FDA completed an inspection of Storz Medical America Inc on June 21, 2017 in Kennesaw, GA. 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 21, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Kennesaw, GA (United States)