FDA Inspection 1017775 — Dermolab Pharma Ltd.

Dermolab Pharma Ltd. — FEI 3003011816

The FDA completed an inspection of Dermolab Pharma Ltd. on June 22, 2017 in Sainte-Julie. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 22, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sainte-Julie (Canada)

Citations

IDCFRDescription
136121 CFR 211.100(a)Absence of Written Procedures