FDA Inspection 1097881 — Medshape, INC.

Medshape, INC. — FEI 3007593722

The FDA completed an inspection of Medshape, INC. on April 16, 2019 in Atlanta, 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
April 16, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Atlanta, GA (United States)