FDA Inspection 1090105 — Laboratoire Atlas Inc.

Laboratoire Atlas Inc. — FEI 3007083710

The FDA completed an inspection of Laboratoire Atlas Inc. on April 26, 2019 in Anjou. 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
April 26, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Anjou (Canada)