FDA Inspection 920348 — Ralston Group

Ralston Group — FEI 3002688031

The FDA completed an inspection of Ralston Group on Apr 2, 2015 in Selma, AL. 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
Apr 2, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Selma, AL (United States)