FDA Inspection 951836 — Gambro Renal Products Inc

Gambro Renal Products Inc — FEI 3006552611

The FDA completed an inspection of Gambro Renal Products Inc on Dec 16, 2015 in Opelika, 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
Dec 16, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Opelika, AL (United States)