FDA Inspection 777935 — ROHO, Inc

ROHO, Inc — FEI 3008630266

The FDA completed an inspection of ROHO, Inc on Apr 19, 2012 in Belleville, IL. 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 19, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Belleville, IL (United States)