FDA Inspection 1116000 — Laboratoires Delon

Laboratoires Delon — FEI 3002698327

The FDA completed an inspection of Laboratoires Delon on January 24, 2020 in Pointe-Claire. 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
January 24, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pointe-Claire (Canada)

Citations

IDCFRDescription
434221 CFR 211.142(b)Storage under appropriate conditions