FDA Inspection 1020360 — Corcym Canada Corp.

Corcym Canada Corp. — FEI 3004478276

The FDA completed an inspection of Corcym Canada Corp. on April 13, 2017 in Burnaby. 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
April 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Burnaby (Canada)

Additional Details

Postmarket Audit Inspections