FDA Inspection 1017775 — Dermolab Pharma Ltd.

Dermolab Pharma Ltd. — FEI 3003011816

The FDA completed an inspection of Dermolab Pharma Ltd. on Jun 22, 2017 in Sainte-Julie. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.