FDA Inspection 933943 — Northern Digital Inc.

Northern Digital Inc. — FEI 3002743211

The FDA completed an inspection of Northern Digital Inc. on July 9, 2015 in Waterloo. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 9, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Waterloo (Canada)