FDA Inspection 1018581 — VIANT PUERTO RICO, INC

VIANT PUERTO RICO, INC — FEI 3010356072

The FDA completed an inspection of VIANT PUERTO RICO, INC on June 2, 2017 in Vega Baja, PR. 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 2, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Vega Baja, PR (United States)