FDA Inspection 1114552 — HK Kolmar Canada, Inc.

HK Kolmar Canada, Inc. — FEI 3002647523

The FDA completed an inspection of HK Kolmar Canada, Inc. on November 1, 2019 in Barrie. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 1, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Barrie (Canada)